| geneid | 284434 |
|---|---|
| ensemblid | ENSG00000188039.17 |
| hgncid | 27619 |
| symbol | NWD1 |
| name | NACHT and WD repeat domain containing 1 |
| refseq_nuc | NM_001007525.5 |
| refseq_prot | NP_001007526.3 |
| ensembl_nuc | ENST00000524140.7 |
| ensembl_prot | ENSP00000428579.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 16719847 |
| end | 16817953 |
| strand | + |
| ver | v1.2 |
| region | chr19:16719847-16817953 |
| region5000 | chr19:16714847-16822953 |
| regionname0 | NWD1_chr19_16719847_16817953 |
| regionname5000 | NWD1_chr19_16714847_16822953 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1432 | 62 | 1 | 10 | 43 | 5 | 2 | 27 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002 | 0/0 | 1432 | 62 | 6 | 29 | 19 | 1 | 7 | 13 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003 | 0/0 | 1432 | 41 | 2 | 11 | 14 | 3 | 11 | 7 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004 | 0/0 | 1432 | 24 | 21 | 1 | 0 | 0 | 2 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005 | 0/0 | 1432 | 21 | 0 | 6 | 8 | 2 | 5 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006 | 0/0 | 1432 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0007 | 0/0 | 1432 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0008 | 0/0 | 1432 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009 | 0/0 | 133 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0010 | 0/0 | 1432 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0011 | 0/0 | 1432 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0012 | 0/0 | 1432 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0013 | 0/0 | 1432 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0014 | 0/0 | 133 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0015 | 0/0 | 1432 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0016 | 0/0 | 1432 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0017 | 0/0 | 1432 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0018 | 0/0 | 1432 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0019 | 0/0 | 1432 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0020 | 0/0 | 1432 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0021 | 0/0 | 1432 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0022 | 0/0 | 1432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0023 | 1/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0024 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0025 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0026 | 0/0 | 1432 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0027 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0028 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0029 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0030 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0031 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0032 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0033 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0034 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0035 | 0/0 | 1432 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0036 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0037 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0038 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0039 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0040 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0041 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0042 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0043 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0044 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0045 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0046 | 0/0 | 1432 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0047 | 0/0 | 1432 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 4299 | 50 | 6 | 26 | 13 | 0 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0002 | 0/1 | 4299 | 49 | 0 | 8 | 34 | 5 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0003 | 0/0 | 4299 | 26 | 2 | 4 | 13 | 2 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0004 | 0/0 | 4299 | 17 | 0 | 5 | 7 | 2 | 3 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0005 | 0/0 | 4299 | 15 | 12 | 1 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0006 | 0/0 | 4299 | 13 | 0 | 6 | 1 | 1 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0007 | 0/0 | 4299 | 10 | 0 | 3 | 5 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0008 | 0/0 | 4299 | 8 | 0 | 2 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0009 | 0/0 | 4299 | 8 | 8 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0010 | 0/0 | 4299 | 6 | 6 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0011 | 0/0 | 4299 | 5 | 5 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0012 | 0/0 | 4299 | 5 | 5 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0013 | 0/0 | 4299 | 4 | 3 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0014 | 0/0 | 4299 | 4 | 3 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0015 | 0/0 | 4299 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0016 | 0/0 | 4299 | 4 | 0 | 1 | 1 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0017 | 0/0 | 4299 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0018 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0019 | 0/0 | 4299 | 3 | 1 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0020 | 0/0 | 4299 | 3 | 0 | 0 | 3 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0021 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0022 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0023 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0024 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0025 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0026 | 0/0 | 4299 | 2 | 0 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0027 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0028 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0029 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0030 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0031 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0032 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0033 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0034 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0035 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0036 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0037 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0038 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0039 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0040 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0041 | 1/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0042 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0043 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0044 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0045 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0046 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0047 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0048 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0049 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0050 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0051 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0052 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0053 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0054 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0055 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0056 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0057 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0058 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0059 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0060 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0061 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0062 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0063 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0064 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0065 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0066 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0067 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0068 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| c0069 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3466 | 77 | 16 | 13 | 31 | 5 | 11 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0002 | 0/0 | 3466 | 68 | 19 | 13 | 26 | 2 | 8 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0003 | 0/0 | 3466 | 27 | 1 | 14 | 3 | 5 | 4 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0004 | 0/0 | 3466 | 19 | 1 | 9 | 7 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0005 | 1/0 | 3466 | 16 | 2 | 3 | 9 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0006 | 0/0 | 3466 | 9 | 9 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0007 | 0/0 | 3466 | 7 | 0 | 1 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0008 | 0/0 | 3465 | 6 | 5 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0009 | 0/0 | 3465 | 6 | 6 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0010 | 0/0 | 3466 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0011 | 0/0 | 3465 | 4 | 3 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0012 | 0/0 | 3466 | 4 | 0 | 0 | 4 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0013 | 0/0 | 3466 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0014 | 0/0 | 3467 | 3 | 0 | 1 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0015 | 0/0 | 3467 | 3 | 0 | 2 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0016 | 0/0 | 3465 | 3 | 1 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0017 | 0/0 | 3464 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0018 | 0/0 | 3466 | 2 | 1 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0019 | 0/0 | 3466 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0020 | 0/0 | 3465 | 2 | 0 | 1 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0021 | 0/0 | 3467 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0022 | 0/0 | 3464 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0023 | 0/0 | 3466 | 2 | 0 | 0 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0024 | 0/0 | 3467 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0025 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0026 | 0/0 | 3464 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0027 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0028 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0029 | 0/0 | 3464 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0030 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0031 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0032 | 0/0 | 3464 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0033 | 0/0 | 3437 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0034 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0035 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0036 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0037 | 0/0 | 3466 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0038 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0039 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0040 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0041 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0042 | 0/0 | 3464 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0043 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0044 | 0/0 | 3466 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0045 | 0/0 | 3465 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0046 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0047 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0048 | 0/0 | 3466 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| t0049 | 0/0 | 3466 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 4299 | 49 | 0 | 8 | 34 | 5 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0008 | 0/0 | 4299 | 8 | 0 | 2 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0022 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0031 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0033 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0035 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001 | 0/0 | 4299 | 50 | 6 | 26 | 13 | 0 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0007 | 0/0 | 4299 | 10 | 0 | 3 | 5 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0046 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0047 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003 | 0/0 | 4299 | 26 | 2 | 4 | 13 | 2 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0006 | 0/0 | 4299 | 13 | 0 | 6 | 1 | 1 | 5 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0059 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0063 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005 | 0/0 | 4299 | 15 | 12 | 1 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0009 | 0/0 | 4299 | 8 | 8 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0060 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0004 | 0/0 | 4299 | 17 | 0 | 5 | 7 | 2 | 3 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0016 | 0/0 | 4299 | 4 | 0 | 1 | 1 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0014 | 0/0 | 4299 | 4 | 3 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0015 | 0/0 | 4299 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0044 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0007c0012 | 0/0 | 4299 | 5 | 5 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0007c0067 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0008c0010 | 0/0 | 4299 | 6 | 6 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0028 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0029 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0068 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0069 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0010c0013 | 0/0 | 4299 | 4 | 3 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0010c0039 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0011c0011 | 0/0 | 4299 | 5 | 5 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0012c0017 | 0/0 | 4299 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0013c0018 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0014c0025 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0014c0054 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0015c0020 | 0/0 | 4299 | 3 | 0 | 0 | 3 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0016c0019 | 0/0 | 4299 | 3 | 1 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0017c0021 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0018c0023 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0019c0024 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0020c0027 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0021c0026 | 0/0 | 4299 | 2 | 0 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0022c0042 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0023c0041 | 1/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0024c0036 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0025c0034 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0026c0040 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0027c0032 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0028c0037 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0029c0038 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0030c0043 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0031c0030 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0032c0053 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0033c0052 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0034c0051 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0035c0050 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0036c0048 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0037c0045 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0038c0049 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0039c0057 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0040c0056 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0041c0065 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0042c0066 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0043c0064 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0044c0058 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0045c0061 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0046c0062 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0047c0055 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 7764 | 24 | 0 | 0 | 18 | 4 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0002 | 0/0 | 7764 | 6 | 0 | 0 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0003 | 0/0 | 7764 | 5 | 0 | 3 | 1 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0004 | 0/0 | 7764 | 3 | 0 | 1 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0005 | 0/0 | 7764 | 3 | 0 | 2 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0007 | 0/0 | 7764 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0011 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0012 | 0/0 | 7764 | 4 | 0 | 0 | 4 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0002t0020 | 0/0 | 7763 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0008t0001 | 0/0 | 7764 | 6 | 0 | 2 | 4 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0008t0002 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0008t0027 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0022t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0022t0002 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0031t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0033t0002 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0001c0035t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0001 | 0/0 | 7764 | 13 | 3 | 6 | 3 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0002 | 0/0 | 7764 | 3 | 2 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0003 | 0/0 | 7764 | 12 | 0 | 9 | 2 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0004 | 0/0 | 7764 | 8 | 1 | 7 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0005 | 0/0 | 7764 | 7 | 0 | 1 | 5 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0014 | 0/0 | 7765 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0020 | 0/0 | 7763 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0021 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0024 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0031 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0001t0033 | 0/0 | 7735 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0007t0001 | 0/0 | 7764 | 5 | 0 | 2 | 1 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0007t0002 | 0/0 | 7764 | 4 | 0 | 1 | 3 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0007t0049 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0046t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0002c0047t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0002 | 0/0 | 7764 | 12 | 1 | 3 | 5 | 1 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0003 | 0/0 | 7764 | 2 | 0 | 0 | 0 | 1 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0004 | 0/0 | 7764 | 6 | 0 | 0 | 4 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0005 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0007 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0024 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0044 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0003t0046 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0006t0001 | 0/0 | 7764 | 3 | 0 | 1 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0006t0002 | 0/0 | 7764 | 9 | 0 | 4 | 1 | 1 | 3 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0006t0038 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0059t0015 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0003c0063t0002 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0006 | 0/0 | 7764 | 7 | 7 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0018 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0022 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0023 | 0/0 | 7764 | 2 | 0 | 0 | 0 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0029 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0039 | 0/0 | 7763 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0005t0048 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0009t0005 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0009t0008 | 0/0 | 7763 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0009t0009 | 0/0 | 7763 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0009t0013 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0009t0036 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0004c0060t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0004t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0004t0002 | 0/0 | 7764 | 7 | 0 | 1 | 6 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0004t0003 | 0/0 | 7764 | 6 | 0 | 2 | 0 | 2 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0004t0004 | 0/0 | 7764 | 2 | 0 | 1 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0004t0021 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0005c0016t0002 | 0/0 | 7764 | 4 | 0 | 1 | 1 | 0 | 2 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0014t0002 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0014t0008 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0014t0009 | 0/0 | 7763 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0015t0006 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0015t0028 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0015t0041 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0006c0044t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0007c0012t0001 | 0/0 | 7764 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0007c0012t0019 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0007c0067t0003 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0008c0010t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0008c0010t0010 | 0/0 | 7764 | 4 | 4 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0008c0010t0047 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0028t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0028t0034 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0029t0002 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0068t0040 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0009c0069t0043 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0010c0013t0008 | 0/0 | 7763 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0010c0013t0009 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0010c0013t0013 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0010c0039t0001 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0011c0011t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0011c0011t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0011c0011t0011 | 0/0 | 7763 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0012c0017t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0012c0017t0002 | 0/0 | 7764 | 3 | 3 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0013c0018t0017 | 0/0 | 7762 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0013c0018t0022 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0014c0025t0002 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0014c0054t0025 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0015c0020t0005 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0015c0020t0007 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0015c0020t0045 | 0/0 | 7763 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0016c0019t0008 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0016c0019t0016 | 0/0 | 7763 | 2 | 0 | 2 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0017c0021t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0017c0021t0002 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0018c0023t0005 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0018c0023t0014 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0019c0024t0001 | 0/0 | 7764 | 2 | 2 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0020c0027t0007 | 0/0 | 7764 | 2 | 0 | 0 | 2 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0021c0026t0002 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0021c0026t0015 | 0/0 | 7765 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0022c0042t0001 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0023c0041t0005 | 1/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0024c0036t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0025c0034t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0026c0040t0002 | 0/0 | 7764 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0027c0032t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0028c0037t0001 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0029c0038t0015 | 0/0 | 7765 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0030c0043t0009 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0031c0030t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0032c0053t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0033c0052t0001 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0034c0051t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0035c0050t0007 | 0/0 | 7764 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0036c0048t0018 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0037c0045t0016 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0038c0049t0042 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0039c0057t0026 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0040c0056t0001 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0041c0065t0032 | 0/0 | 7762 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0042c0066t0008 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0043c0064t0002 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0044c0058t0035 | 0/0 | 7764 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0045c0061t0003 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0046c0062t0030 | 0/0 | 7763 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| a0047c0055t0037 | 0/0 | 7764 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | copy fasta | chr19 | 16714847 | 16822953 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0153 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0005g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0007g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0007g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0012g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0012g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0012g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0002t0020g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0008t0027g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0022t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0022t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0031t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0033t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0001c0035t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0014g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0020g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0021g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0024g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0031g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0001t0033g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0007t0049g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0046t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0002c0047t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0004g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0024g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0044g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0003t0046g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0006t0038g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0059t0015g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0003c0063t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0018g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0022g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0023g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0023g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0029g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0039g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0005t0048g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0013g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0009t0036g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0004c0060t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0004t0021g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0016t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0016t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0016t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0005c0016t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0014t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0014t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0014t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0014t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0015t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0015t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0015t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0015t0041g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0006c0044t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0007c0012t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0007c0012t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0007c0012t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0007c0012t0019g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0007c0012t0019g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0007c0067t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0008c0010t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0008c0010t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0008c0010t0010g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0008c0010t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0008c0010t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0008c0010t0047g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0009c0028t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0009c0028t0034g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0009c0029t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0009c0029t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0009c0068t0040g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0009c0069t0043g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0010c0013t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0010c0013t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0010c0013t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0010c0013t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0010c0039t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0011c0011t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0011c0011t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0011c0011t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0011c0011t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0011c0011t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0012c0017t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0012c0017t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0012c0017t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0012c0017t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0013c0018t0017g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0013c0018t0017g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0013c0018t0022g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0014c0025t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0014c0025t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0014c0054t0025g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0015c0020t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0015c0020t0007g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0015c0020t0045g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0016c0019t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0016c0019t0016g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0016c0019t0016g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0017c0021t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0017c0021t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0017c0021t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0018c0023t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0018c0023t0014g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0019c0024t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0019c0024t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0020c0027t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0020c0027t0007g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0021c0026t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0021c0026t0015g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0022c0042t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0023c0041t0005g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0024c0036t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0025c0034t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0026c0040t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0027c0032t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0028c0037t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0029c0038t0015g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0030c0043t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0031c0030t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0032c0053t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0033c0052t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0034c0051t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0035c0050t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0036c0048t0018g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0037c0045t0016g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0038c0049t0042g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0039c0057t0026g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0040c0056t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0041c0065t0032g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0042c0066t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0043c0064t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0044c0058t0035g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0045c0061t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0046c0062t0030g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| a0047c0055t0037g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0046 | t0001 | g0219 | EUR | GBR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0157 | EUR | GBR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00280 | hp1 | a0005 | c0004 | t0003 | g0248 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0154 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00323 | hp1 | a0005 | c0004 | t0003 | g0280 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0146 | EUR | FIN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00544 | hp1 | a0005 | c0004 | t0002 | g0042 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00558 | hp1 | a0002 | c0001 | t0005 | g0245 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00558 | hp2 | a0005 | c0004 | t0002 | g0103 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00597 | hp1 | a0003 | c0003 | t0046 | g0077 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00597 | hp2 | a0002 | c0001 | t0021 | g0150 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00609 | hp1 | a0003 | c0003 | t0004 | g0062 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00639 | hp1 | a0002 | c0007 | t0001 | g0221 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00639 | hp2 | a0005 | c0004 | t0003 | g0272 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00642 | hp1 | a0003 | c0006 | t0002 | g0072 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00642 | hp2 | a0010 | c0039 | t0001 | g0161 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | CHS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00733 | hp1 | a0003 | c0006 | t0002 | g0086 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00733 | hp2 | a0005 | c0004 | t0021 | g0275 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00735 | hp1 | a0002 | c0001 | t0004 | g0108 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00735 | hp2 | a0010 | c0013 | t0008 | g0194 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00738 | hp1 | a0001 | c0008 | t0001 | g0270 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG00738 | hp2 | a0003 | c0006 | t0002 | g0096 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01070 | hp1 | a0016 | c0019 | t0016 | g0004 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01070 | hp2 | a0002 | c0001 | t0004 | g0112 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01071 | hp1 | a0002 | c0001 | t0024 | g0109 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01071 | hp2 | a0016 | c0019 | t0016 | g0003 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01074 | hp1 | a0005 | c0016 | t0002 | g0101 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0159 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01081 | hp1 | a0004 | c0005 | t0039 | g0084 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01081 | hp2 | a0002 | c0001 | t0004 | g0107 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01099 | hp1 | a0003 | c0006 | t0001 | g0128 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01099 | hp2 | a0001 | c0002 | t0020 | g0249 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01109 | hp1 | a0002 | c0001 | t0001 | g0160 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01109 | hp2 | a0006 | c0014 | t0002 | g0015 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0261 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01167 | hp2 | a0005 | c0004 | t0002 | g0039 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01175 | hp1 | a0003 | c0059 | t0015 | g0037 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0267 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01192 | hp1 | a0002 | c0001 | t0004 | g0111 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01192 | hp2 | a0003 | c0003 | t0044 | g0070 | AMR | PUR | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01256 | hp1 | a0002 | c0007 | t0002 | g0110 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0144 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01257 | hp1 | a0005 | c0004 | t0004 | g0097 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01257 | hp2 | a0002 | c0001 | t0033 | g0216 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01261 | hp1 | a0002 | c0001 | t0003 | g0220 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01261 | hp2 | a0002 | c0001 | t0004 | g0113 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01346 | hp1 | a0002 | c0001 | t0003 | g0162 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01346 | hp2 | a0001 | c0002 | t0005 | g0287 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01358 | hp1 | a0002 | c0001 | t0005 | g0184 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01358 | hp2 | a0001 | c0008 | t0001 | g0168 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01361 | hp1 | a0026 | c0040 | t0002 | g0036 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01361 | hp2 | a0021 | c0026 | t0015 | g0078 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01433 | hp1 | a0003 | c0003 | t0002 | g0060 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01433 | hp2 | a0002 | c0001 | t0014 | g0238 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01496 | hp1 | a0022 | c0042 | t0001 | g0152 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01496 | hp2 | a0005 | c0004 | t0003 | g0266 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01516 | hp1 | a0003 | c0003 | t0002 | g0091 | EUR | IBS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0163 | EUR | IBS | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01884 | hp1 | a0006 | c0015 | t0028 | g0204 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01884 | hp2 | a0017 | c0021 | t0001 | g0231 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01891 | hp1 | a0001 | c0035 | t0002 | g0020 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01891 | hp2 | a0009 | c0029 | t0002 | g0298 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01934 | hp1 | a0001 | c0002 | t0003 | g0200 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0164 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01943 | hp1 | a0002 | c0001 | t0003 | g0195 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01943 | hp2 | a0002 | c0001 | t0003 | g0236 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01975 | hp1 | a0001 | c0002 | t0007 | g0041 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01975 | hp2 | a0002 | c0001 | t0004 | g0035 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01978 | hp1 | a0003 | c0003 | t0002 | g0085 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0171 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01981 | hp1 | a0002 | c0001 | t0003 | g0176 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01981 | hp2 | a0003 | c0006 | t0002 | g0100 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0011 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02004 | hp2 | a0002 | c0001 | t0003 | g0190 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02015 | hp1 | a0001 | c0002 | t0011 | g0105 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02015 | hp2 | a0003 | c0003 | t0004 | g0079 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02027 | hp1 | a0028 | c0037 | t0001 | g0223 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02027 | hp2 | a0002 | c0001 | t0014 | g0187 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02040 | hp2 | a0018 | c0023 | t0014 | g0149 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02055 | hp1 | a0038 | c0049 | t0042 | g0054 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02055 | hp2 | a0004 | c0005 | t0048 | g0002 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02056 | hp2 | a0003 | c0003 | t0002 | g0068 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02071 | hp2 | a0020 | c0027 | t0007 | g0069 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02074 | hp2 | a0003 | c0003 | t0007 | g0064 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0271 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0067 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02083 | hp1 | a0020 | c0027 | t0007 | g0080 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02083 | hp2 | a0001 | c0002 | t0004 | g0009 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02129 | hp1 | a0003 | c0003 | t0004 | g0073 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02132 | hp2 | a0002 | c0007 | t0002 | g0122 | EAS | KHV | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02145 | hp1 | a0011 | c0011 | t0002 | g0022 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02145 | hp2 | a0030 | c0043 | t0009 | g0023 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02148 | hp1 | a0002 | c0001 | t0003 | g0237 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02148 | hp2 | a0003 | c0006 | t0038 | g0106 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02155 | hp2 | a0002 | c0001 | t0005 | g0155 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02165 | hp2 | a0005 | c0004 | t0002 | g0074 | EAS | CDX | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02257 | hp1 | a0012 | c0017 | t0001 | g0212 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02257 | hp2 | a0009 | c0029 | t0002 | g0297 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02258 | hp1 | a0004 | c0005 | t0018 | g0256 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02258 | hp2 | a0004 | c0005 | t0022 | g0050 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02273 | hp1 | a0002 | c0001 | t0003 | g0185 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02273 | hp2 | a0002 | c0001 | t0004 | g0032 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02280 | hp1 | a0012 | c0017 | t0002 | g0038 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02280 | hp2 | a0014 | c0025 | t0002 | g0048 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02293 | hp1 | a0021 | c0026 | t0002 | g0083 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02293 | hp2 | a0001 | c0002 | t0005 | g0192 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02300 | hp1 | a0002 | c0001 | t0003 | g0183 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0147 | AMR | PEL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02451 | hp1 | a0007 | c0012 | t0001 | g0234 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02451 | hp2 | a0032 | c0053 | t0001 | g0252 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02572 | hp1 | a0004 | c0005 | t0006 | g0227 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02572 | hp2 | a0009 | c0028 | t0034 | g0258 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02602 | hp1 | a0002 | c0001 | t0003 | g0215 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02602 | hp2 | a0003 | c0063 | t0002 | g0098 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02615 | hp1 | a0004 | c0005 | t0006 | g0229 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02615 | hp2 | a0046 | c0062 | t0030 | g0250 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02622 | hp1 | a0006 | c0015 | t0041 | g0053 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02622 | hp2 | a0019 | c0024 | t0001 | g0259 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02630 | hp1 | a0002 | c0001 | t0001 | g0263 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02630 | hp2 | a0004 | c0005 | t0006 | g0226 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02647 | hp1 | a0008 | c0010 | t0010 | g0284 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02647 | hp2 | a0006 | c0015 | t0006 | g0290 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02698 | hp1 | a0003 | c0006 | t0001 | g0281 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02698 | hp2 | a0003 | c0003 | t0004 | g0026 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02723 | hp1 | a0006 | c0015 | t0006 | g0293 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02723 | hp2 | a0017 | c0021 | t0002 | g0051 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02735 | hp1 | a0005 | c0016 | t0002 | g0056 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02735 | hp2 | a0005 | c0004 | t0003 | g0283 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02809 | hp1 | a0010 | c0013 | t0013 | g0173 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02809 | hp2 | a0008 | c0010 | t0010 | g0278 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02818 | hp1 | a0041 | c0065 | t0032 | g0166 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02818 | hp2 | a0002 | c0001 | t0002 | g0029 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02886 | hp1 | a0004 | c0060 | t0002 | g0125 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02886 | hp2 | a0004 | c0009 | t0008 | g0286 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02895 | hp1 | a0004 | c0005 | t0006 | g0230 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02895 | hp2 | a0003 | c0003 | t0002 | g0117 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02896 | hp1 | a0009 | c0068 | t0040 | g0116 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02896 | hp2 | a0012 | c0017 | t0002 | g0018 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02897 | hp1 | a0004 | c0005 | t0006 | g0228 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02897 | hp2 | a0012 | c0017 | t0002 | g0019 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02922 | hp1 | a0042 | c0066 | t0008 | g0264 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02922 | hp2 | a0007 | c0012 | t0001 | g0232 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02965 | hp1 | a0009 | c0028 | t0002 | g0115 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02965 | hp2 | a0006 | c0014 | t0008 | g0253 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03041 | hp1 | a0004 | c0009 | t0005 | g0140 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03041 | hp2 | a0002 | c0001 | t0001 | g0260 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03098 | hp1 | a0013 | c0018 | t0017 | g0295 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03098 | hp2 | a0004 | c0009 | t0008 | g0205 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03130 | hp1 | a0004 | c0009 | t0009 | g0052 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03130 | hp2 | a0008 | c0010 | t0010 | g0131 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03139 | hp1 | a0007 | c0012 | t0001 | g0235 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03139 | hp2 | a0004 | c0005 | t0006 | g0225 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03195 | hp1 | a0011 | c0011 | t0011 | g0024 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03195 | hp2 | a0008 | c0010 | t0047 | g0005 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03209 | hp1 | a0014 | c0054 | t0025 | g0118 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03209 | hp2 | a0010 | c0013 | t0013 | g0172 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03225 | hp1 | a0007 | c0012 | t0019 | g0292 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03225 | hp2 | a0006 | c0014 | t0009 | g0016 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03239 | hp1 | a0040 | c0056 | t0001 | g0279 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03239 | hp2 | a0005 | c0004 | t0001 | g0274 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03453 | hp1 | a0004 | c0009 | t0005 | g0224 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03453 | hp2 | a0019 | c0024 | t0001 | g0251 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03486 | hp1 | a0007 | c0012 | t0019 | g0233 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0262 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03490 | hp1 | a0031 | c0030 | t0001 | g0158 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03490 | hp2 | a0004 | c0005 | t0023 | g0095 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03491 | hp1 | a0003 | c0006 | t0002 | g0061 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03491 | hp2 | a0002 | c0007 | t0001 | g0213 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03492 | hp1 | a0004 | c0005 | t0023 | g0094 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03492 | hp2 | a0002 | c0007 | t0001 | g0217 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03516 | hp1 | a0017 | c0021 | t0002 | g0046 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03516 | hp2 | a0007 | c0067 | t0003 | g0277 | AFR | ESN | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03540 | hp1 | a0009 | c0069 | t0043 | g0299 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03540 | hp2 | a0004 | c0009 | t0036 | g0126 | AFR | GWD | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03579 | hp1 | a0004 | c0005 | t0001 | g0296 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03579 | hp2 | a0004 | c0009 | t0013 | g0206 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03654 | hp1 | a0003 | c0003 | t0004 | g0075 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03654 | hp2 | a0003 | c0006 | t0001 | g0282 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03688 | hp1 | a0001 | c0031 | t0001 | g0156 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03688 | hp2 | a0002 | c0001 | t0005 | g0169 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03710 | hp1 | a0003 | c0006 | t0002 | g0082 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03710 | hp2 | a0005 | c0004 | t0003 | g0273 | SAS | PJL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03834 | hp1 | a0036 | c0048 | t0018 | g0129 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03834 | hp2 | a0002 | c0001 | t0020 | g0289 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03927 | hp1 | a0027 | c0032 | t0001 | g0269 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0180 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04115 | hp1 | a0003 | c0006 | t0002 | g0092 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04115 | hp2 | a0002 | c0001 | t0031 | g0214 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04184 | hp1 | a0003 | c0003 | t0003 | g0288 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04184 | hp2 | a0003 | c0003 | t0002 | g0065 | SAS | BEB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04199 | hp1 | a0047 | c0055 | t0037 | g0088 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04228 | hp1 | a0005 | c0016 | t0002 | g0058 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG04228 | hp2 | a0003 | c0003 | t0002 | g0066 | SAS | STU | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18522 | hp1 | a0016 | c0019 | t0008 | g0257 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0210 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18747 | hp1 | a0001 | c0002 | t0005 | g0130 | EAS | CHB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18747 | hp2 | a0002 | c0007 | t0049 | g0132 | EAS | CHB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18906 | hp1 | a0044 | c0058 | t0035 | g0167 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18906 | hp2 | a0033 | c0052 | t0001 | g0254 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18945 | hp1 | a0001 | c0002 | t0012 | g0188 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18945 | hp2 | a0003 | c0003 | t0002 | g0076 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18946 | hp1 | a0001 | c0002 | t0012 | g0203 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18946 | hp2 | a0015 | c0020 | t0005 | g0222 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18951 | hp1 | a0015 | c0020 | t0045 | g0121 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18952 | hp1 | a0001 | c0002 | t0012 | g0178 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18952 | hp2 | a0002 | c0001 | t0003 | g0177 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18954 | hp1 | a0018 | c0023 | t0005 | g0240 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18954 | hp2 | a0003 | c0003 | t0002 | g0089 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18960 | hp1 | a0002 | c0007 | t0001 | g0239 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18960 | hp2 | a0002 | c0001 | t0005 | g0241 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18962 | hp1 | a0003 | c0003 | t0005 | g0141 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18962 | hp2 | a0001 | c0033 | t0002 | g0012 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18966 | hp1 | a0003 | c0003 | t0024 | g0087 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18968 | hp2 | a0002 | c0001 | t0005 | g0246 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18971 | hp2 | a0002 | c0001 | t0003 | g0182 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18973 | hp1 | a0003 | c0006 | t0002 | g0071 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18975 | hp1 | a0005 | c0004 | t0002 | g0093 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18980 | hp1 | a0001 | c0008 | t0001 | g0134 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18980 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18982 | hp1 | a0005 | c0004 | t0002 | g0059 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18982 | hp2 | a0001 | c0008 | t0027 | g0136 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18993 | hp1 | a0001 | c0022 | t0002 | g0102 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA18993 | hp2 | a0029 | c0038 | t0015 | g0055 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19003 | hp1 | a0001 | c0002 | t0012 | g0198 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19003 | hp2 | a0003 | c0003 | t0004 | g0099 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19005 | hp1 | a0001 | c0008 | t0001 | g0145 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19005 | hp2 | a0005 | c0004 | t0004 | g0090 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19007 | hp1 | a0001 | c0008 | t0001 | g0135 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19009 | hp1 | a0001 | c0022 | t0001 | g0151 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19009 | hp2 | a0002 | c0001 | t0002 | g0043 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19011 | hp1 | a0001 | c0008 | t0002 | g0044 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19030 | hp1 | a0014 | c0025 | t0002 | g0049 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19030 | hp2 | a0010 | c0013 | t0009 | g0045 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19043 | hp1 | a0006 | c0044 | t0001 | g0255 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19043 | hp2 | a0004 | c0005 | t0029 | g0265 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19060 | hp1 | a0024 | c0036 | t0001 | g0209 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19066 | hp1 | a0035 | c0050 | t0007 | g0104 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19066 | hp2 | a0005 | c0004 | t0002 | g0120 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19068 | hp2 | a0002 | c0047 | t0001 | g0138 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19070 | hp1 | a0002 | c0007 | t0002 | g0057 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19070 | hp2 | a0002 | c0001 | t0005 | g0244 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19074 | hp2 | a0001 | c0002 | t0007 | g0030 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19077 | hp1 | a0002 | c0007 | t0002 | g0008 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19077 | hp2 | a0015 | c0020 | t0007 | g0119 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19080 | hp1 | a0005 | c0016 | t0002 | g0081 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19085 | hp2 | a0001 | c0008 | t0001 | g0139 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19087 | hp1 | a0025 | c0034 | t0001 | g0133 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19240 | hp1 | a0006 | c0014 | t0009 | g0014 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA19240 | hp2 | a0002 | c0001 | t0002 | g0021 | AFR | YRI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20129 | hp1 | a0008 | c0010 | t0002 | g0114 | AFR | ASW | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20129 | hp2 | a0008 | c0010 | t0010 | g0276 | AFR | ASW | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20752 | hp1 | a0003 | c0006 | t0002 | g0027 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20752 | hp2 | a0045 | c0061 | t0003 | g0285 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20805 | hp1 | a0003 | c0003 | t0003 | g0143 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0165 | EUR | TSI | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01123 | hp1 | a0002 | c0007 | t0001 | g0040 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG01123 | hp2 | a0003 | c0003 | t0002 | g0127 | AMR | CLM | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02109 | hp1 | a0011 | c0011 | t0011 | g0017 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02109 | hp2 | a0037 | c0045 | t0016 | g0001 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02559 | hp1 | a0011 | c0011 | t0011 | g0025 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG02559 | hp2 | a0004 | c0005 | t0006 | g0211 | AFR | ACB | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03471 | hp1 | a0013 | c0018 | t0017 | g0294 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG03471 | hp2 | a0004 | c0009 | t0009 | g0047 | AFR | MSL | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG06807 | hp1 | a0043 | c0064 | t0002 | g0300 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| HG06807 | hp2 | a0002 | c0001 | t0004 | g0034 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20300 | hp1 | a0013 | c0018 | t0022 | g0124 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA20300 | hp2 | a0039 | c0057 | t0026 | g0202 | AFR | USA | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA21309 | hp1 | a0034 | c0051 | t0002 | g0028 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| NA21309 | hp2 | a0011 | c0011 | t0001 | g0247 | AFR | LWK | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0153 | REF | REF | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| homoSapiens_grch38 | hp1 | a0023 | c0041 | t0005 | g0243 | REF | REF | NWD1_chr19_16714847_16822953 | NWD1 | chr19 | 16714847 | 16822953 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16731241
|
G | T | 21 | a0003a0004a0005others(18): Show | 130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
missense_variant | MODERATE | c.44G>T | p.Cys15Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/19 | 595/7764 | 44/4299 | 15/1432 | chr19 | 16731241 | ||
| chr19:16736665
|
T | C | 1 | a0047 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.113T>C | p.Ile38Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/19 | 664/7764 | 113/4299 | 38/1432 | chr19 | 16736665 | ||
| chr19:16744429
|
C | G | 2 | a0009a0014 | 9 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.207C>G | p.Ile69Met | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 758/7764 | 207/4299 | 69/1432 | chr19 | 16744429 | ||
| chr19:16744454
|
A | G | 28 | a0002a0003a0004others(25): Show | 187 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(184): Show |
missense_variant | MODERATE | c.232A>G | p.Ile78Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 783/7764 | 232/4299 | 78/1432 | chr19 | 16744454 | ||
| chr19:16744622
|
G | T | 2 | a0009a0014 | 9 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(6): Show |
stop_gained | HIGH | c.400G>T | p.Glu134* | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 951/7764 | 400/4299 | 134/1432 | chr19 | 16744622 | ||
| chr19:16744646
|
C | T | 2 | a0007a0032 | 7 | HG02451.hp1 HG02451.hp2 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.424C>T | p.Arg142Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 975/7764 | 424/4299 | 142/1432 | chr19 | 16744646 | ||
| chr19:16744655
|
G | A | 1 | a0031 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.433G>A | p.Ala145Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 984/7764 | 433/4299 | 145/1432 | chr19 | 16744655 | ||
| chr19:16744661
|
G | A | 1 | a0013 | 3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.439G>A | p.Glu147Lys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/19 | 990/7764 | 439/4299 | 147/1432 | chr19 | 16744661 | ||
| chr19:16749159
|
C | T | 1 | a0030 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.517C>T | p.Arg173Trp | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1068/7764 | 517/4299 | 173/1432 | chr19 | 16749159 | ||
| chr19:16749190
|
A | T | 2 | a0008a0033 | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
missense_variant | MODERATE | c.548A>T | p.Gln183Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1099/7764 | 548/4299 | 183/1432 | chr19 | 16749190 | ||
| chr19:16749273
|
C | T | 10 | a0008a0009a0019others(7): Show | 20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
missense_variant | MODERATE | c.631C>T | p.Leu211Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1182/7764 | 631/4299 | 211/1432 | chr19 | 16749273 | ||
| chr19:16749276
|
G | A | 2 | a0008a0033 | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
missense_variant | MODERATE | c.634G>A | p.Ala212Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1185/7764 | 634/4299 | 212/1432 | chr19 | 16749276 | ||
| chr19:16749280
|
A | T | 1 | a0014 | 2 | HG02280.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.638A>T | p.Asp213Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1189/7764 | 638/4299 | 213/1432 | chr19 | 16749280 | ||
| chr19:16749294
|
G | A | 42 | a0001a0002a0003others(39): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
missense_variant | MODERATE | c.652G>A | p.Ala218Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1203/7764 | 652/4299 | 218/1432 | chr19 | 16749294 | ||
| chr19:16749616
|
A | G | 1 | a0029 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.974A>G | p.Gln325Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1525/7764 | 974/4299 | 325/1432 | chr19 | 16749616 | ||
| chr19:16749747
|
G | A | 10 | a0008a0009a0019others(7): Show | 20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
missense_variant | MODERATE | c.1105G>A | p.Val369Ile | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1656/7764 | 1105/4299 | 369/1432 | chr19 | 16749747 | ||
| chr19:16749865
|
A | G | 1 | a0028 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1223A>G | p.Asp408Gly | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1774/7764 | 1223/4299 | 408/1432 | chr19 | 16749865 | ||
| chr19:16749874
|
C | T | 2 | a0008a0033 | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
missense_variant | MODERATE | c.1232C>T | p.Thr411Ile | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1783/7764 | 1232/4299 | 411/1432 | chr19 | 16749874 | ||
| chr19:16749979
|
G | A | 1 | a0036 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1337G>A | p.Arg446His | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1888/7764 | 1337/4299 | 446/1432 | chr19 | 16749979 | ||
| chr19:16750071
|
G | A | 1 | a0021 | 2 | HG01361.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.1429G>A | p.Asp477Asn | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1980/7764 | 1429/4299 | 477/1432 | chr19 | 16750071 | ||
| chr19:16750084
|
G | A | 3 | a0039a0041a0042 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1442G>A | p.Arg481Gln | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1993/7764 | 1442/4299 | 481/1432 | chr19 | 16750084 | ||
| chr19:16750273
|
G | A | 1 | a0041 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1631G>A | p.Arg544Gln | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 2182/7764 | 1631/4299 | 544/1432 | chr19 | 16750273 | ||
| chr19:16750396
|
A | G | 1 | a0020 | 2 | HG02071.hp2 HG02083.hp1 |
missense_variant | MODERATE | c.1754A>G | p.Tyr585Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 2305/7764 | 1754/4299 | 585/1432 | chr19 | 16750396 | ||
| chr19:16759232
|
C | G | 1 | a0038 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1777C>G | p.Leu593Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/19 | 2328/7764 | 1777/4299 | 593/1432 | chr19 | 16759232 | ||
| chr19:16759236
|
C | T | 1 | a0024 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.1781C>T | p.Ser594Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/19 | 2332/7764 | 1781/4299 | 594/1432 | chr19 | 16759236 | ||
| chr19:16761998
|
C | T | 1 | a0025 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.1993C>T | p.Arg665Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/19 | 2544/7764 | 1993/4299 | 665/1432 | chr19 | 16761998 | ||
| chr19:16763861
|
G | T | 1 | a0017 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.2167G>T | p.Val723Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/19 | 2718/7764 | 2167/4299 | 723/1432 | chr19 | 16763861 | ||
| chr19:16779432
|
C | G | 18 | a0004a0006a0008others(15): Show | 67 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(64): Show |
missense_variant | MODERATE | c.2698C>G | p.Gln900Glu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/19 | 3249/7764 | 2698/4299 | 900/1432 | chr19 | 16779432 | ||
| chr19:16789027
|
A | T | 46 | a0001a0002a0003others(43): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
missense_variant | MODERATE | c.2777A>T | p.Asn926Ile | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/19 | 3328/7764 | 2777/4299 | 926/1432 | chr19 | 16789027 | ||
| chr19:16789053
|
C | A | 1 | a0012 | 4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
missense_variant | MODERATE | c.2803C>A | p.His935Asn | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/19 | 3354/7764 | 2803/4299 | 935/1432 | chr19 | 16789053 | ||
| chr19:16789054
|
A | G | 21 | a0004a0006a0008others(18): Show | 75 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(72): Show |
missense_variant | MODERATE | c.2804A>G | p.His935Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/19 | 3355/7764 | 2804/4299 | 935/1432 | chr19 | 16789054 | ||
| chr19:16799964
|
G | A | 1 | a0017 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.3538G>A | p.Gly1180Ser | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/19 | 4089/7764 | 3538/4299 | 1180/1432 | chr19 | 16799964 | ||
| chr19:16800060
|
C | G | 3 | a0009a0019a0043 | 5 | HG01891.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
missense_variant | MODERATE | c.3634C>G | p.Leu1212Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/19 | 4185/7764 | 3634/4299 | 1212/1432 | chr19 | 16800060 | ||
| chr19:16800142
|
C | T | 1 | a0027 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.3716C>T | p.Thr1239Ile | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/19 | 4267/7764 | 3716/4299 | 1239/1432 | chr19 | 16800142 | ||
| chr19:16807648
|
C | T | 1 | a0026 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.3799C>T | p.Arg1267Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4350/7764 | 3799/4299 | 1267/1432 | chr19 | 16807648 | ||
| chr19:16807733
|
C | A | 1 | a0044 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.3884C>A | p.Pro1295His | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4435/7764 | 3884/4299 | 1295/1432 | chr19 | 16807733 | ||
| chr19:16807738
|
G | A | 2 | a0039a0041 | 2 | HG02818.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.3889G>A | p.Glu1297Lys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4440/7764 | 3889/4299 | 1297/1432 | chr19 | 16807738 | ||
| chr19:16807782
|
G | T | 1 | a0040 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3933G>T | p.Glu1311Asp | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4484/7764 | 3933/4299 | 1311/1432 | chr19 | 16807782 | ||
| chr19:16807957
|
G | T | 1 | a0045 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.4108G>T | p.Asp1370Tyr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4659/7764 | 4108/4299 | 1370/1432 | chr19 | 16807957 | ||
| chr19:16808107
|
C | T | 2 | a0039a0041 | 2 | HG02818.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.4258C>T | p.Arg1420Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4809/7764 | 4258/4299 | 1420/1432 | chr19 | 16808107 | ||
| chr19:16817953
|
A | C | 2 | a0004a0006 | 11 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
splice_region_variant | LOW | c.*2914A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | chr19 | 16817953 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16749372
|
C | T | 3 | a0039c0057a0041c0065a0042c0066 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.730C>T | p.Leu244Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1281/7764 | 730/4299 | 244/1432 | chr19 | 16749372 | ||
| chr19:16749383
|
C | T | 1 | a0039c0057 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.741C>T | p.Ser247Ser | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1292/7764 | 741/4299 | 247/1432 | chr19 | 16749383 | ||
| chr19:16749581
|
C | T | 10 | a0004c0005a0006c0015a0009c0068others(7): Show | 32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
synonymous_variant | LOW | c.939C>T | p.Cys313Cys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1490/7764 | 939/4299 | 313/1432 | chr19 | 16749581 | ||
| chr19:16749737
|
G | A | 5 | a0004c0009a0006c0014a0010c0013others(2): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
synonymous_variant | LOW | c.1095G>A | p.Lys365Lys | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1646/7764 | 1095/4299 | 365/1432 | chr19 | 16749737 | ||
| chr19:16749791
|
T | C | 12 | a0008c0010a0009c0028a0009c0029others(9): Show | 20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
synonymous_variant | LOW | c.1149T>C | p.Arg383Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 1700/7764 | 1149/4299 | 383/1432 | chr19 | 16749791 | ||
| chr19:16750130
|
C | T | 1 | a0002c0047 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.1488C>T | p.Ser496Ser | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/19 | 2039/7764 | 1488/4299 | 496/1432 | chr19 | 16750130 | ||
| chr19:16759333
|
C | T | 2 | a0001c0035a0007c0012 | 6 | HG01891.hp1 HG02451.hp1 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.1878C>T | p.Phe626Phe | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/19 | 2429/7764 | 1878/4299 | 626/1432 | chr19 | 16759333 | ||
| chr19:16761983
|
C | T | 2 | a0002c0046a0003c0063 | 2 | HG00099.hp1 HG02602.hp2 |
synonymous_variant | LOW | c.1978C>T | p.Leu660Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/19 | 2529/7764 | 1978/4299 | 660/1432 | chr19 | 16761983 | ||
| chr19:16762129
|
G | A | 44 | a0001c0008a0001c0022a0001c0031others(41): Show | 117 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(114): Show |
synonymous_variant | LOW | c.2124G>A | p.Leu708Leu | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/19 | 2675/7764 | 2124/4299 | 708/1432 | chr19 | 16762129 | ||
| chr19:16765183
|
C | A | 1 | a0044c0058 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.2401C>A | p.Arg801Arg | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/19 | 2952/7764 | 2401/4299 | 801/1432 | chr19 | 16765183 | ||
| chr19:16789118
|
C | T | 2 | a0001c0022a0017c0021 | 5 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(2): Show |
synonymous_variant | LOW | c.2868C>T | p.Pro956Pro | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/19 | 3419/7764 | 2868/4299 | 956/1432 | chr19 | 16789118 | ||
| chr19:16797862
|
G | A | 1 | a0001c0031 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.3435G>A | p.Thr1145Thr | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/19 | 3986/7764 | 3435/4299 | 1145/1432 | chr19 | 16797862 | ||
| chr19:16807674
|
G | A | 1 | a0003c0059 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.3825G>A | p.Val1275Val | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4376/7764 | 3825/4299 | 1275/1432 | chr19 | 16807674 | ||
| chr19:16807734
|
T | C | 1 | a0044c0058 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.3885T>C | p.Pro1295Pro | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4436/7764 | 3885/4299 | 1295/1432 | chr19 | 16807734 | ||
| chr19:16807851
|
G | A | 1 | a0001c0033 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.4002G>A | p.Pro1334Pro | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/19 | 4553/7764 | 4002/4299 | 1334/1432 | chr19 | 16807851 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16719935
|
C | T | 1 | a0002c0007t0049 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-463C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11263 | chr19 | 16719935 | |||||
| chr19:16719936
|
G | A | 1 | a0014c0054t0025 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-462G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11262 | chr19 | 16719936 | |||||
| chr19:16719993
|
C | T | 4 | a0004c0005t0048a0008c0010t0047a0016c0019t0016others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-405C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | chr19 | 16719993 | ||||||
| chr19:16720033
|
C | T | 1 | a0001c0002t0012 | 4 | NA18945.hp1 NA18946.hp1 NA18952.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-365C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11165 | chr19 | 16720033 | |||||
| chr19:16720144
|
G | A | 4 | a0004c0005t0048a0008c0010t0047a0016c0019t0016others(1): Show | 5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-254G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | 11054 | chr19 | 16720144 | |||||
| chr19:16720249
|
C | T | 60 | a0001c0002t0002a0001c0002t0004a0001c0002t0007others(57): Show | 125 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(122): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-149C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | chr19 | 16720249 | ||||||
| chr19:16720250
|
G | A | 1 | a0039c0057t0026 | 1 | NA20300.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-148G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/19 | chr19 | 16720250 | ||||||
| chr19:16815101
|
C | T | 1 | a0044c0058t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*62C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 62 | chr19 | 16815101 | |||||
| chr19:16815256
|
A | T | 17 | a0001c0002t0003a0001c0002t0004a0002c0001t0003others(14): Show | 53 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*217A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 217 | chr19 | 16815256 | |||||
| chr19:16815530
|
C | A | 1 | a0044c0058t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*491C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 491 | chr19 | 16815530 | |||||
| chr19:16815636
|
C | T | 2 | a0039c0057t0026a0041c0065t0032 | 2 | HG02818.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*597C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 597 | chr19 | 16815636 | |||||
| chr19:16815856
|
G | A | 121 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(118): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*817G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 817 | chr19 | 16815856 | |||||
| chr19:16815930
|
G | A | 1 | a0004c0009t0036 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*891G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 891 | chr19 | 16815930 | |||||
| chr19:16815936
|
T | G | 3 | a0004c0005t0022a0013c0018t0017a0013c0018t0022 | 4 | HG02258.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*897T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 897 | chr19 | 16815936 | |||||
| chr19:16815946
|
G | A | 1 | a0047c0055t0037 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 907 | chr19 | 16815946 | |||||
| chr19:16815947
|
G | T | 3 | a0001c0002t0020a0002c0001t0020a0003c0003t0044 | 3 | HG01099.hp2 HG01192.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*908G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 908 | chr19 | 16815947 | |||||
| chr19:16815974
|
C | T | 2 | a0008c0010t0010a0009c0069t0043 | 5 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*935C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 935 | chr19 | 16815974 | |||||
| chr19:16816217
|
C | T | 1 | a0009c0028t0034 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1178C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1178 | chr19 | 16816217 | |||||
| chr19:16816407
|
CA | C | 15 | a0004c0009t0008a0004c0009t0009a0004c0009t0013others(12): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1369delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1369 | chr19 | 16816407 | |||||
| chr19:16816620
|
T | C | 1 | a0003c0006t0038 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1581T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1581 | chr19 | 16816620 | |||||
| chr19:16816663
|
T | C | 1 | a0044c0058t0035 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1624T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1624 | chr19 | 16816663 | |||||
| chr19:16816684
|
TC | T | 4 | a0004c0005t0029a0038c0049t0042a0039c0057t0026others(1): Show | 4 | HG02055.hp1 HG02818.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1646delC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1646 | chr19 | 16816684 | |||||
| chr19:16816720
|
G | A | 4 | a0004c0005t0018a0004c0005t0023a0004c0005t0039others(1): Show | 5 | HG01081.hp1 HG02258.hp1 HG03490.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1681G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1681 | chr19 | 16816720 | |||||
| chr19:16816945
|
A | G | 1 | a0003c0003t0046 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1906A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1906 | chr19 | 16816945 | |||||
| chr19:16816984
|
C | T | 15 | a0004c0009t0008a0004c0009t0009a0004c0009t0013others(12): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1945C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 1945 | chr19 | 16816984 | |||||
| chr19:16817299
|
CATA | C | 3 | a0004c0005t0022a0013c0018t0017a0013c0018t0022 | 4 | HG02258.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2275_*2277delAAT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2275 | INFO_REALIGN_3_PRIME | chr19 | 16817299 | ||||
| chr19:16817329
|
G | A | 3 | a0004c0005t0022a0013c0018t0017a0013c0018t0022 | 4 | HG02258.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2290G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2290 | chr19 | 16817329 | |||||
| chr19:16817334
|
C | T | 1 | a0006c0015t0028 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2295C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2295 | chr19 | 16817334 | |||||
| chr19:16817341
|
CTGTAATC others(22): Show |
C | 1 | a0002c0001t0033 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303_*2331delTGTA others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2303 | chr19 | 16817341 | |||||
| chr19:16817376
|
G | A | 2 | a0009c0068t0040a0014c0054t0025 | 2 | HG02896.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2337G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2337 | chr19 | 16817376 | |||||
| chr19:16817417
|
A | G | 1 | a0046c0062t0030 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2378A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2378 | chr19 | 16817417 | |||||
| chr19:16817569
|
T | C | 1 | a0002c0001t0031 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2530T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2530 | chr19 | 16817569 | |||||
| chr19:16817598
|
C | CA | 14 | a0002c0001t0014a0002c0001t0021a0002c0001t0024others(11): Show | 17 | HG00597.hp2 HG00733.hp2 HG01071.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2579dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2580 | INFO_REALIGN_3_PRIME | chr19 | 16817598 | ||||
| chr19:16817598
|
CA | C | 11 | a0001c0002t0011a0001c0002t0020a0001c0008t0027others(8): Show | 13 | HG01081.hp1 HG01099.hp2 HG02015.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2579delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2579 | INFO_REALIGN_3_PRIME | chr19 | 16817598 | ||||
| chr19:16817701
|
G | T | 1 | a0007c0012t0019 | 2 | HG03225.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2662G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 19/19 | 2662 | chr19 | 16817701 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16720318
|
AT | A | 5 | a0004c0005t0048g0002a0008c0010t0047g0005a0016c0019t0016g0003others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+26delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720318 | ||||||
| chr19:16720324
|
C | T | 5 | a0004c0005t0048g0002a0008c0010t0047g0005a0016c0019t0016g0003others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+31C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720324 | ||||||
| chr19:16720444
|
A | C | 5 | a0004c0005t0048g0002a0008c0010t0047g0005a0016c0019t0016g0003others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-105+151A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720444 | ||||||
| chr19:16720490
|
A | G | 4 | a0009c0029t0002g0297a0009c0029t0002g0298a0009c0069t0043g0299others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+197A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720490 | ||||||
| chr19:16720567
|
T | A | 126 | a0001c0002t0002g0007a0001c0002t0002g0010a0001c0002t0002g0013others(123): Show | 126 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.-105+274T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720567 | ||||||
| chr19:16720703
|
C | T | 4 | a0003c0003t0002g0127a0004c0009t0036g0126a0004c0060t0002g0125others(1): Show | 4 | HG01123.hp2 HG02886.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+410C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720703 | ||||||
| chr19:16720734
|
T | C | 1 | a0003c0006t0001g0128 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-105+441T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720734 | ||||||
| chr19:16720845
|
A | G | 136 | a0001c0002t0002g0007a0001c0002t0002g0010a0001c0002t0002g0013others(133): Show | 136 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.-105+552A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720845 | ||||||
| chr19:16720848
|
T | C | 136 | a0001c0002t0002g0007a0001c0002t0002g0010a0001c0002t0002g0013others(133): Show | 136 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.-105+555T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720848 | ||||||
| chr19:16720878
|
C | G | 1 | a0001c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-105+585C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720878 | ||||||
| chr19:16720903
|
C | T | 1 | a0001c0002t0001g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-105+610C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720903 | ||||||
| chr19:16720904
|
G | A | 1 | a0036c0048t0018g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-105+611G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720904 | ||||||
| chr19:16720914
|
G | C | 1 | a0001c0002t0005g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-105+621G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16720914 | ||||||
| chr19:16721069
|
C | T | 87 | a0001c0002t0002g0063a0001c0002t0002g0123a0001c0002t0011g0105others(84): Show | 87 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.-105+776C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721069 | ||||||
| chr19:16721094
|
C | G | 4 | a0002c0007t0002g0122a0005c0004t0002g0120a0015c0020t0007g0119others(1): Show | 4 | HG02132.hp2 NA18951.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+801C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721094 | ||||||
| chr19:16721395
|
C | G | 177 | a0001c0002t0001g0268a0001c0002t0001g0271a0001c0002t0002g0007others(174): Show | 177 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.-105+1102C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721395 | ||||||
| chr19:16721414
|
C | T | 1 | a0006c0015t0006g0290 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-105+1121C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721414 | ||||||
| chr19:16721480
|
G | C | 11 | a0004c0005t0022g0050a0004c0009t0009g0047a0004c0009t0009g0052others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-105+1187G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721480 | ||||||
| chr19:16721673
|
G | C | 292 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(289): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-105+1380G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721673 | ||||||
| chr19:16721892
|
C | T | 1 | a0001c0002t0007g0041 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-105+1599C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721892 | ||||||
| chr19:16721915
|
A | G | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-105+1622A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16721915 | ||||||
| chr19:16722114
|
T | C | 132 | a0001c0002t0002g0007a0001c0002t0002g0010a0001c0002t0002g0013others(129): Show | 132 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-105+1821T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722114 | ||||||
| chr19:16722115
|
GAAA | G | 132 | a0001c0002t0002g0007a0001c0002t0002g0010a0001c0002t0002g0013others(129): Show | 132 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.-105+1827_-105+182 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16722115 | |||||
| chr19:16722120
|
A | C | 3 | a0002c0001t0003g0237a0002c0001t0014g0238a0002c0001t0020g0289 | 3 | HG01433.hp2 HG02148.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-105+1827A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722120 | ||||||
| chr19:16722123
|
C | A | 17 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(14): Show | 17 | HG01070.hp1 HG01071.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.-105+1830C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722123 | ||||||
| chr19:16722170
|
T | C | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-105+1877T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722170 | ||||||
| chr19:16722205
|
G | A | 11 | a0004c0005t0022g0050a0004c0009t0009g0047a0004c0009t0009g0052others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-105+1912G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722205 | ||||||
| chr19:16722251
|
A | G | 4 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(1): Show | 4 | HG01167.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+1958A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722251 | ||||||
| chr19:16722255
|
T | C | 4 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(1): Show | 4 | HG01167.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+1962T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722255 | ||||||
| chr19:16722256
|
G | A | 4 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(1): Show | 4 | HG01167.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-105+1963G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722256 | ||||||
| chr19:16722260
|
C | T | 8 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(5): Show | 8 | HG01167.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-105+1967C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722260 | ||||||
| chr19:16722271
|
C | G | 1 | a0002c0001t0003g0236 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-105+1978C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722271 | ||||||
| chr19:16722310
|
A | G | 4 | a0003c0003t0002g0117a0008c0010t0002g0114a0009c0028t0002g0115others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105+2017A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722310 | ||||||
| chr19:16722490
|
T | C | 58 | a0001c0002t0002g0063a0001c0002t0002g0123a0001c0002t0011g0105others(55): Show | 58 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-104-1876T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722490 | ||||||
| chr19:16722531
|
C | T | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-104-1835C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722531 | ||||||
| chr19:16722591
|
C | T | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-104-1775C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722591 | ||||||
| chr19:16722647
|
A | G | 1 | a0009c0069t0043g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-104-1719A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722647 | ||||||
| chr19:16722935
|
G | C | 1 | a0002c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104-1431G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16722935 | ||||||
| chr19:16723128
|
C | T | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-104-1238C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723128 | ||||||
| chr19:16723129
|
G | A | 12 | a0003c0003t0002g0117a0004c0005t0022g0050a0004c0009t0009g0047others(9): Show | 12 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-104-1237G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723129 | ||||||
| chr19:16723181
|
G | A | 1 | a0029c0038t0015g0055 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-104-1185G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723181 | ||||||
| chr19:16723230
|
G | A | 1 | a0006c0015t0006g0290 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-104-1136G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723230 | ||||||
| chr19:16723261
|
C | T | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-104-1105C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723261 | ||||||
| chr19:16723423
|
C | A | 1 | a0005c0016t0002g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-104-943C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723423 | ||||||
| chr19:16723423
|
C | G | 3 | a0004c0005t0001g0296a0012c0017t0002g0038a0013c0018t0022g0124 | 3 | HG02280.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-104-943C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723423 | ||||||
| chr19:16723521
|
C | T | 8 | a0004c0005t0022g0050a0004c0009t0009g0047a0004c0009t0009g0052others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104-845C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723521 | ||||||
| chr19:16723626
|
A | C | 125 | a0001c0002t0002g0031a0001c0002t0002g0063a0001c0002t0002g0123others(122): Show | 125 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.-104-740A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723626 | ||||||
| chr19:16723676
|
C | CTGTTT | 17 | a0002c0001t0005g0246a0002c0001t0014g0238a0003c0003t0002g0127others(14): Show | 17 | HG01109.hp2 HG01123.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-104-652_-104-648d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | |||||
| chr19:16723676
|
C | CTGTTTTG others(3): Show |
1 | a0026c0040t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-104-657_-104-648d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | |||||
| chr19:16723676
|
CTGTTT | C | 97 | a0001c0002t0002g0063a0001c0002t0002g0123a0001c0002t0020g0249others(94): Show | 97 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.-104-652_-104-648d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | |||||
| chr19:16723676
|
CTGTTTTG others(3): Show |
C | 19 | a0003c0003t0002g0117a0004c0005t0001g0296a0004c0005t0022g0050others(16): Show | 19 | HG02258.hp2 HG02280.hp2 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.-104-657_-104-648d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | |||||
| chr19:16723676
|
CTGTTTTG others(8): Show |
C | 2 | a0012c0017t0002g0038a0014c0054t0025g0118 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-104-662_-104-648d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr19 | 16723676 | |||||
| chr19:16723730
|
C | T | 8 | a0004c0005t0006g0225a0004c0005t0006g0226a0004c0005t0006g0227others(5): Show | 8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-104-636C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723730 | ||||||
| chr19:16723913
|
C | G | 2 | a0001c0002t0005g0130a0028c0037t0001g0223 | 2 | HG02027.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-104-453C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723913 | ||||||
| chr19:16723943
|
G | A | 59 | a0001c0002t0002g0063a0001c0002t0002g0123a0001c0022t0002g0102others(56): Show | 59 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-104-423G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16723943 | ||||||
| chr19:16724089
|
T | C | 1 | a0001c0002t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-104-277T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 1/18 | chr19 | 16724089 | ||||||
| chr19:16724470
|
G | A | 1 | a0018c0023t0005g0240 | 1 | NA18954.hp1 | splice_region_variant&intron_variant | LOW | c.-7+7G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724470 | ||||||
| chr19:16724660
|
T | A | 2 | a0004c0005t0029g0265a0042c0066t0008g0264 | 2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-7+197T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724660 | ||||||
| chr19:16724751
|
T | C | 8 | a0004c0005t0022g0050a0004c0009t0009g0047a0004c0009t0009g0052others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+288T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724751 | ||||||
| chr19:16724880
|
G | T | 1 | a0009c0028t0034g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7+417G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16724880 | ||||||
| chr19:16725007
|
TA | T | 94 | a0001c0002t0002g0031a0001c0002t0002g0063a0001c0002t0002g0123others(91): Show | 94 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-7+545delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725007 | ||||||
| chr19:16725008
|
AT | A | 27 | a0001c0002t0020g0249a0001c0035t0002g0020a0002c0001t0002g0021others(24): Show | 27 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.-7+551delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725008 | |||||
| chr19:16725050
|
C | T | 1 | a0002c0007t0001g0221 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-7+587C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725050 | ||||||
| chr19:16725133
|
C | T | 1 | a0002c0001t0003g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-7+670C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725133 | ||||||
| chr19:16725158
|
C | T | 1 | a0002c0046t0001g0219 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-7+695C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725158 | ||||||
| chr19:16725326
|
T | A | 1 | a0005c0016t0002g0058 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-7+863T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725326 | ||||||
| chr19:16725386
|
G | A | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-7+923G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725386 | ||||||
| chr19:16725536
|
A | G | 2 | a0003c0003t0002g0127a0004c0009t0036g0126 | 2 | HG01123.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-7+1073A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725536 | ||||||
| chr19:16725577
|
G | A | 5 | a0004c0009t0009g0047a0004c0009t0009g0052a0017c0021t0002g0046others(2): Show | 5 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+1114G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725577 | ||||||
| chr19:16725651
|
C | G | 1 | a0001c0002t0005g0130 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-7+1188C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725651 | ||||||
| chr19:16725656
|
G | A | 4 | a0003c0003t0002g0117a0008c0010t0002g0114a0009c0028t0002g0115others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+1193G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725656 | ||||||
| chr19:16725755
|
G | T | 21 | a0001c0002t0020g0249a0001c0035t0002g0020a0002c0001t0002g0021others(18): Show | 21 | HG00280.hp1 HG01099.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+1292G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725755 | ||||||
| chr19:16725834
|
C | T | 21 | a0001c0002t0002g0031a0001c0002t0004g0033a0001c0002t0007g0030others(18): Show | 21 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+1371C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725834 | ||||||
| chr19:16725919
|
A | T | 1 | a0002c0001t0002g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-7+1456A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725919 | ||||||
| chr19:16725945
|
GT | G | 113 | a0001c0002t0002g0031a0001c0002t0002g0063a0001c0002t0002g0123others(110): Show | 113 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.-7+1492delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725945 | |||||
| chr19:16725960
|
G | GT | 7 | a0001c0002t0001g0218a0002c0001t0003g0215a0002c0001t0031g0214others(4): Show | 7 | HG01257.hp2 HG02056.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+1506dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725960 | |||||
| chr19:16725961
|
T | G | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-7+1498T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725961 | ||||||
| chr19:16725964
|
T | G | 8 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+1501T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725964 | ||||||
| chr19:16725970
|
G | T | 1 | a0012c0017t0002g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7+1507G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725970 | ||||||
| chr19:16725971
|
C | G | 1 | a0012c0017t0002g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7+1508C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725971 | ||||||
| chr19:16725971
|
CT | C | 90 | a0001c0002t0002g0031a0001c0002t0002g0063a0001c0002t0002g0123others(87): Show | 90 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.-7+1517delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16725971 | |||||
| chr19:16725972
|
T | C | 1 | a0012c0017t0002g0038 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7+1509T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16725972 | ||||||
| chr19:16726050
|
C | T | 3 | a0006c0014t0008g0253a0006c0044t0001g0255a0033c0052t0001g0254 | 3 | HG02965.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-7+1587C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726050 | ||||||
| chr19:16726081
|
G | A | 3 | a0004c0005t0018g0256a0009c0028t0034g0258a0037c0045t0016g0001 | 3 | HG02109.hp2 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-7+1618G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726081 | ||||||
| chr19:16726086
|
C | T | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+1623C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726086 | ||||||
| chr19:16726326
|
G | A | 1 | a0005c0004t0002g0059 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-7+1863G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726326 | ||||||
| chr19:16726518
|
C | T | 4 | a0009c0029t0002g0297a0009c0029t0002g0298a0009c0069t0043g0299others(1): Show | 4 | HG01361.hp1 HG01891.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7+2055C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726518 | ||||||
| chr19:16726522
|
C | T | 1 | a0011c0011t0011g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7+2059C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726522 | ||||||
| chr19:16726588
|
C | T | 58 | a0001c0002t0002g0063a0001c0002t0002g0123a0001c0022t0002g0102others(55): Show | 58 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-7+2125C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726588 | ||||||
| chr19:16726691
|
G | C | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-7+2228G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16726691 | ||||||
| chr19:16727008
|
T | C | 4 | a0003c0003t0002g0117a0008c0010t0002g0114a0009c0028t0002g0115others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+2545T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727008 | ||||||
| chr19:16727016
|
G | A | 1 | a0001c0035t0002g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-7+2553G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727016 | ||||||
| chr19:16727078
|
A | G | 3 | a0004c0005t0001g0296a0012c0017t0002g0038a0013c0018t0022g0124 | 3 | HG02280.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-7+2615A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727078 | ||||||
| chr19:16727112
|
C | T | 3 | a0003c0003t0001g0210a0004c0005t0006g0211a0012c0017t0001g0212 | 3 | HG02257.hp1 HG02559.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-7+2649C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727112 | ||||||
| chr19:16727132
|
A | G | 58 | a0001c0002t0002g0063a0001c0002t0002g0123a0001c0022t0002g0102others(55): Show | 58 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-7+2669A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727132 | ||||||
| chr19:16727240
|
G | A | 1 | a0003c0003t0002g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-7+2777G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727240 | ||||||
| chr19:16727252
|
G | C | 4 | a0003c0003t0002g0117a0008c0010t0002g0114a0009c0028t0002g0115others(1): Show | 4 | HG02895.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+2789G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727252 | ||||||
| chr19:16727441
|
G | A | 5 | a0004c0009t0009g0047a0004c0009t0009g0052a0017c0021t0002g0046others(2): Show | 5 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2978G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727441 | ||||||
| chr19:16727526
|
G | T | 20 | a0001c0002t0002g0031a0001c0002t0004g0033a0001c0002t0007g0030others(17): Show | 20 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-7+3063G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727526 | ||||||
| chr19:16727551
|
C | T | 1 | a0024c0036t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-7+3088C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727551 | ||||||
| chr19:16727562
|
G | A | 1 | a0002c0001t0002g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-7+3099G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727562 | ||||||
| chr19:16727592
|
C | G | 5 | a0004c0009t0009g0047a0004c0009t0009g0052a0017c0021t0002g0046others(2): Show | 5 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+3129C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727592 | ||||||
| chr19:16727649
|
A | G | 2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG00673.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.-7+3186A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727649 | ||||||
| chr19:16727681
|
G | T | 3 | a0003c0003t0002g0117a0009c0028t0002g0115a0009c0068t0040g0116 | 3 | HG02895.hp2 HG02896.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-7+3218G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727681 | ||||||
| chr19:16727689
|
T | G | 1 | a0005c0004t0003g0248 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-7+3226T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727689 | ||||||
| chr19:16727698
|
G | A | 8 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(5): Show | 8 | HG01109.hp2 HG01167.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+3235G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727698 | ||||||
| chr19:16727776
|
G | A | 30 | a0001c0002t0001g0146a0001c0002t0001g0148a0001c0002t0001g0153others(27): Show | 30 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.-7+3313G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727776 | ||||||
| chr19:16727789
|
T | C | 1 | a0002c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7+3326T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727789 | ||||||
| chr19:16727831
|
C | T | 20 | a0001c0002t0002g0031a0001c0002t0004g0033a0001c0002t0007g0030others(17): Show | 20 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-6-3361C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727831 | ||||||
| chr19:16727951
|
A | G | 1 | a0001c0002t0001g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-6-3241A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727951 | ||||||
| chr19:16727994
|
G | A | 4 | a0012c0017t0002g0018a0012c0017t0002g0019a0041c0065t0032g0166others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-3198G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16727994 | ||||||
| chr19:16728106
|
T | C | 12 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(9): Show | 12 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-6-3086T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728106 | ||||||
| chr19:16728219
|
C | T | 1 | a0038c0049t0042g0054 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-6-2973C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728219 | ||||||
| chr19:16728220
|
G | A | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-6-2972G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728220 | ||||||
| chr19:16728281
|
C | CT | 75 | a0001c0002t0001g0218a0001c0002t0001g0268a0001c0002t0001g0271others(72): Show | 75 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-6-2892dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728281 | |||||
| chr19:16728281
|
CT | C | 80 | a0001c0002t0002g0063a0001c0002t0002g0123a0001c0002t0003g0144others(77): Show | 80 | HG00280.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-6-2892delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728281 | |||||
| chr19:16728324
|
G | A | 1 | a0002c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-6-2868G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728324 | ||||||
| chr19:16728631
|
C | T | 6 | a0004c0009t0009g0047a0004c0009t0009g0052a0008c0010t0002g0114others(3): Show | 6 | HG02723.hp2 HG03130.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-2561C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728631 | ||||||
| chr19:16728710
|
C | T | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-6-2482C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728710 | ||||||
| chr19:16728719
|
C | A | 1 | a0001c0008t0001g0168 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-6-2473C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728719 | ||||||
| chr19:16728726
|
C | T | 3 | a0016c0019t0008g0257a0016c0019t0016g0003a0016c0019t0016g0004 | 3 | HG01070.hp1 HG01071.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-6-2466C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728726 | ||||||
| chr19:16728747
|
A | C | 1 | a0001c0002t0001g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-6-2445A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728747 | ||||||
| chr19:16728817
|
G | A | 4 | a0004c0005t0022g0050a0014c0025t0002g0048a0014c0025t0002g0049others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-2375G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728817 | ||||||
| chr19:16728851
|
A | G | 2 | a0001c0002t0001g0199a0001c0002t0003g0200 | 2 | HG01934.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-6-2341A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728851 | ||||||
| chr19:16728931
|
A | G | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-6-2261A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728931 | ||||||
| chr19:16728943
|
CA | C | 69 | a0001c0002t0001g0268a0001c0002t0001g0271a0001c0002t0003g0267others(66): Show | 69 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-6-2228delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728943 | |||||
| chr19:16728943
|
CAA | C | 92 | a0001c0002t0002g0063a0001c0002t0020g0249a0001c0035t0002g0020others(89): Show | 92 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.-6-2229_-6-2228del others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728943 | |||||
| chr19:16728943
|
CAAA | C | 8 | a0004c0005t0022g0050a0004c0005t0023g0094a0004c0005t0023g0095others(5): Show | 8 | HG01074.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-2230_-6-2228del others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728943 | |||||
| chr19:16728960
|
A | T | 21 | a0001c0002t0020g0249a0001c0035t0002g0020a0002c0001t0001g0263others(18): Show | 21 | HG01099.hp2 HG01175.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6-2232A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728960 | ||||||
| chr19:16728961
|
A | T | 2 | a0008c0010t0047g0005a0014c0054t0025g0118 | 2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-6-2231A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728961 | ||||||
| chr19:16728963
|
AAT | A | 6 | a0004c0005t0006g0225a0004c0009t0009g0047a0017c0021t0002g0046others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6-2227_-6-2226del others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16728963 | |||||
| chr19:16728965
|
T | A | 1 | a0001c0002t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-6-2227T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16728965 | ||||||
| chr19:16729405
|
C | G | 1 | a0001c0002t0005g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-6-1787C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729405 | ||||||
| chr19:16729545
|
G | A | 2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-6-1647G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729545 | ||||||
| chr19:16729577
|
T | TAAAAAAA others(6): Show |
3 | a0006c0015t0006g0293a0013c0018t0017g0294a0013c0018t0017g0295 | 3 | HG02723.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-6-1611_-6-1599dup others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | |||||
| chr19:16729577
|
T | TAAAAAAA others(7): Show |
8 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(5): Show | 8 | HG01167.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6-1612_-6-1599dup others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | |||||
| chr19:16729577
|
T | TAAAAAAA others(8): Show |
7 | a0006c0014t0002g0015a0006c0014t0009g0014a0006c0015t0006g0290others(4): Show | 7 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-1613_-6-1599dup others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | |||||
| chr19:16729577
|
TA | T | 11 | a0001c0002t0012g0198a0001c0002t0012g0203a0004c0005t0006g0225others(8): Show | 11 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6-1599delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729577 | |||||
| chr19:16729627
|
C | T | 1 | a0005c0004t0002g0093 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-6-1565C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729627 | ||||||
| chr19:16729644
|
G | A | 1 | a0001c0002t0001g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-6-1548G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729644 | ||||||
| chr19:16729790
|
A | G | 1 | a0001c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-6-1402A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729790 | ||||||
| chr19:16729905
|
A | AGAAG | 23 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(20): Show | 23 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-6-1263_-6-1260dup others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729905 | |||||
| chr19:16729905
|
AGAAG | A | 10 | a0001c0002t0020g0249a0006c0014t0008g0253a0006c0044t0001g0255others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.-6-1263_-6-1260del others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16729905 | |||||
| chr19:16729959
|
C | T | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-6-1233C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16729959 | ||||||
| chr19:16730040
|
T | C | 3 | a0009c0029t0002g0297a0009c0029t0002g0298a0009c0069t0043g0299 | 3 | HG01891.hp2 HG02257.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6-1152T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730040 | ||||||
| chr19:16730045
|
C | T | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-1147C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730045 | ||||||
| chr19:16730050
|
G | A | 1 | a0002c0001t0005g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-6-1142G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730050 | ||||||
| chr19:16730061
|
C | T | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-1131C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730061 | ||||||
| chr19:16730138
|
A | G | 2 | a0004c0005t0018g0256a0004c0009t0008g0286 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-6-1054A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730138 | ||||||
| chr19:16730253
|
C | A | 1 | a0004c0005t0048g0002 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-6-939C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730253 | ||||||
| chr19:16730254
|
A | G | 61 | a0001c0002t0020g0249a0003c0003t0001g0210a0003c0003t0002g0127others(58): Show | 61 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-6-938A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730254 | ||||||
| chr19:16730305
|
A | C | 1 | a0001c0002t0004g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-6-887A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730305 | ||||||
| chr19:16730461
|
C | T | 2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-6-731C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730461 | ||||||
| chr19:16730515
|
G | A | 26 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(23): Show | 26 | HG01109.hp2 HG01167.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-6-677G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730515 | ||||||
| chr19:16730568
|
A | G | 157 | a0001c0002t0020g0249a0002c0001t0001g0260a0002c0001t0001g0261others(154): Show | 157 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.-6-624A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730568 | ||||||
| chr19:16730674
|
ACCACTGC | A | 5 | a0001c0035t0002g0020a0011c0011t0002g0022a0011c0011t0011g0024others(2): Show | 5 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6-515_-6-509delAC others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16730674 | |||||
| chr19:16730732
|
T | A | 1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-6-460T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730732 | ||||||
| chr19:16730733
|
A | T | 61 | a0003c0003t0002g0006a0003c0003t0002g0060a0003c0003t0002g0065others(58): Show | 61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-6-459A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730733 | ||||||
| chr19:16730911
|
C | CT | 125 | a0002c0001t0004g0032a0002c0001t0004g0034a0002c0001t0004g0035others(122): Show | 125 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.-6-264dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16730911 | |||||
| chr19:16730911
|
CT | C | 16 | a0001c0008t0001g0145a0002c0001t0001g0260a0002c0001t0001g0261others(13): Show | 16 | HG01109.hp2 HG01167.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-6-264delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16730911 | |||||
| chr19:16730914
|
T | TC | 3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-6-278_-6-277insC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730914 | ||||||
| chr19:16730981
|
C | T | 2 | a0003c0006t0002g0092a0005c0016t0002g0058 | 2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-6-211C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16730981 | ||||||
| chr19:16731020
|
A | G | 68 | a0003c0003t0001g0210a0003c0003t0002g0117a0003c0003t0002g0127others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.-6-172A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 2/18 | chr19 | 16731020 | ||||||
| chr19:16731296
|
C | T | 1 | a0013c0018t0022g0124 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+18C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731296 | ||||||
| chr19:16731299
|
G | C | 7 | a0004c0005t0006g0225a0004c0009t0009g0047a0008c0010t0010g0131others(4): Show | 7 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+21G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731299 | ||||||
| chr19:16731314
|
T | A | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.81+36T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731314 | ||||||
| chr19:16731410
|
G | A | 26 | a0001c0002t0020g0249a0002c0001t0001g0260a0002c0001t0001g0261others(23): Show | 26 | HG01099.hp2 HG01109.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+132G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731410 | ||||||
| chr19:16731414
|
C | T | 1 | a0045c0061t0003g0285 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.81+136C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731414 | ||||||
| chr19:16731440
|
G | A | 61 | a0003c0003t0002g0006a0003c0003t0002g0060a0003c0003t0002g0065others(58): Show | 61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.81+162G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731440 | ||||||
| chr19:16731451
|
C | T | 130 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+173C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731451 | ||||||
| chr19:16731556
|
C | T | 61 | a0003c0003t0002g0006a0003c0003t0002g0060a0003c0003t0002g0065others(58): Show | 61 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.81+278C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731556 | ||||||
| chr19:16731568
|
A | G | 130 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+290A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731568 | ||||||
| chr19:16731601
|
A | G | 131 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(128): Show | 131 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.81+323A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731601 | ||||||
| chr19:16731610
|
C | CTT | 63 | a0003c0003t0002g0006a0003c0003t0002g0060a0003c0003t0002g0065others(60): Show | 63 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.81+343_81+344dupTT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16731610 | |||||
| chr19:16731610
|
C | CTTT | 60 | a0003c0003t0001g0210a0003c0003t0002g0127a0003c0003t0003g0143others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.81+342_81+344dupTT others(1): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16731610 | |||||
| chr19:16731610
|
C | CTTTT | 7 | a0003c0003t0002g0117a0009c0028t0002g0115a0009c0028t0034g0258others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+341_81+344dupTT others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16731610 | |||||
| chr19:16731636
|
G | A | 1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+358G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731636 | ||||||
| chr19:16731666
|
G | A | 16 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(13): Show | 16 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+388G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731666 | ||||||
| chr19:16731689
|
T | C | 131 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(128): Show | 131 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.81+411T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731689 | ||||||
| chr19:16731715
|
T | C | 130 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+437T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731715 | ||||||
| chr19:16731717
|
G | A | 1 | a0026c0040t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.81+439G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731717 | ||||||
| chr19:16731754
|
G | A | 130 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+476G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731754 | ||||||
| chr19:16731767
|
T | G | 130 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+489T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731767 | ||||||
| chr19:16731854
|
C | T | 130 | a0003c0003t0001g0210a0003c0003t0002g0006a0003c0003t0002g0060others(127): Show | 130 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.81+576C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731854 | ||||||
| chr19:16731929
|
A | G | 60 | a0003c0003t0002g0006a0003c0003t0002g0060a0003c0003t0002g0065others(57): Show | 60 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.81+651A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16731929 | ||||||
| chr19:16732078
|
G | A | 2 | a0002c0007t0002g0008a0002c0007t0002g0057 | 2 | NA19070.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.81+800G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732078 | ||||||
| chr19:16732100
|
C | G | 1 | a0001c0002t0002g0031 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.81+822C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732100 | ||||||
| chr19:16732216
|
C | CA | 6 | a0001c0002t0001g0170a0001c0002t0003g0267a0002c0001t0001g0171others(3): Show | 6 | HG01175.hp2 HG01361.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+956dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732216 | |||||
| chr19:16732216
|
CAA | C | 78 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(75): Show | 78 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.81+955_81+956delAA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732216 | |||||
| chr19:16732216
|
CAAA | C | 68 | a0003c0003t0001g0210a0003c0003t0002g0117a0003c0003t0002g0127others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.81+954_81+956delAA others(1): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732216 | |||||
| chr19:16732351
|
G | C | 2 | a0006c0015t0028g0204a0034c0051t0002g0028 | 2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.81+1073G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732351 | ||||||
| chr19:16732397
|
G | C | 1 | a0001c0002t0001g0146 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.81+1119G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732397 | ||||||
| chr19:16732433
|
C | T | 151 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(148): Show | 151 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.81+1155C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732433 | ||||||
| chr19:16732438
|
T | C | 1 | a0011c0011t0002g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.81+1160T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732438 | ||||||
| chr19:16732516
|
G | A | 2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.81+1238G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732516 | ||||||
| chr19:16732568
|
C | G | 143 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1290C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732568 | ||||||
| chr19:16732598
|
A | ATTTT | 13 | a0002c0001t0001g0260a0003c0003t0003g0143a0003c0003t0007g0064others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | ||||||
| chr19:16732598
|
A | ATTTTT | 94 | a0002c0001t0001g0261a0002c0001t0001g0262a0002c0001t0004g0032others(91): Show | 94 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | ||||||
| chr19:16732598
|
A | ATTTTTT | 32 | a0003c0003t0002g0089a0003c0003t0002g0091a0003c0003t0002g0127others(29): Show | 32 | HG01123.hp2 HG01175.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | ||||||
| chr19:16732598
|
A | ATTTTTTT | 4 | a0004c0005t0006g0230a0004c0005t0018g0256a0004c0009t0009g0047others(1): Show | 4 | HG02258.hp1 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+1320_81+1321ins others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732598 | ||||||
| chr19:16732599
|
A | AT | 10 | a0001c0002t0001g0201a0002c0001t0004g0111a0003c0003t0002g0117others(7): Show | 10 | HG01192.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+1336dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732599 | |||||
| chr19:16732599
|
A | T | 143 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1321A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732599 | ||||||
| chr19:16732654
|
C | CAAAAA | 8 | a0003c0003t0002g0085a0003c0003t0004g0026a0003c0003t0024g0087others(5): Show | 8 | HG00733.hp1 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+1387_81+1391dup others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAA | 46 | a0002c0001t0004g0032a0002c0001t0004g0034a0002c0001t0004g0035others(43): Show | 46 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.81+1386_81+1391dup others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA | 24 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(21): Show | 24 | HG00323.hp1 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+1385_81+1391dup others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA others(1): Show |
40 | a0003c0003t0003g0143a0003c0006t0001g0281a0003c0006t0001g0282others(37): Show | 40 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.81+1384_81+1391dup others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA others(2): Show |
12 | a0003c0003t0003g0288a0004c0005t0006g0226a0004c0005t0006g0227others(9): Show | 12 | HG00280.hp1 HG00639.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+1383_81+1391dup others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA others(3): Show |
2 | a0003c0003t0001g0210a0003c0003t0002g0127 | 2 | HG01123.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.81+1382_81+1391dup others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA others(5): Show |
1 | a0046c0062t0030g0250 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+1380_81+1391dup others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA others(6): Show |
3 | a0004c0005t0006g0225a0017c0021t0002g0051a0043c0064t0002g0300 | 3 | HG02723.hp2 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.81+1379_81+1391dup others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA others(7): Show |
2 | a0004c0009t0009g0047a0008c0010t0010g0131 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.81+1378_81+1391dup others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732654
|
C | CAAAAAAA others(8): Show |
1 | a0017c0021t0002g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81+1377_81+1391dup others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732654 | |||||
| chr19:16732658
|
A | AAAAAAAA others(6): Show |
3 | a0001c0002t0020g0249a0002c0001t0001g0147a0006c0015t0028g0204 | 3 | HG01099.hp2 HG01884.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.81+1391_81+1392ins others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732658 | |||||
| chr19:16732658
|
A | AAAAAAAA others(5): Show |
13 | a0003c0003t0002g0117a0006c0014t0008g0253a0006c0044t0001g0255others(10): Show | 13 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+1386_81+1397dup others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732658 | |||||
| chr19:16732658
|
A | AAAAAAAA others(4): Show |
1 | a0032c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.81+1390_81+1391ins others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732658 | |||||
| chr19:16732670
|
G | A | 143 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1392G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732670 | ||||||
| chr19:16732673
|
A | AAAAAAAA others(6): Show |
1 | a0004c0005t0001g0296 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.81+1397_81+1398ins others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16732673 | |||||
| chr19:16732676
|
G | A | 60 | a0003c0003t0001g0210a0003c0003t0002g0127a0003c0003t0003g0143others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.81+1398G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732676 | ||||||
| chr19:16732677
|
T | A | 143 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1399T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732677 | ||||||
| chr19:16732716
|
C | A | 2 | a0010c0013t0013g0172a0010c0013t0013g0173 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.81+1438C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732716 | ||||||
| chr19:16732722
|
G | C | 150 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(147): Show | 150 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.81+1444G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732722 | ||||||
| chr19:16732743
|
T | C | 2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.81+1465T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732743 | ||||||
| chr19:16732787
|
G | A | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.81+1509G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732787 | ||||||
| chr19:16732847
|
C | T | 10 | a0001c0035t0002g0020a0002c0001t0001g0263a0002c0001t0002g0021others(7): Show | 10 | HG01891.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+1569C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732847 | ||||||
| chr19:16732876
|
G | C | 160 | a0001c0002t0020g0249a0002c0001t0001g0147a0002c0001t0001g0260others(157): Show | 160 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(157): Show |
intron_variant | MODIFIER | c.81+1598G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732876 | ||||||
| chr19:16732890
|
G | A | 143 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(140): Show | 143 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+1612G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732890 | ||||||
| chr19:16732902
|
GA | G | 7 | a0003c0003t0002g0117a0009c0028t0002g0115a0009c0028t0034g0258others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+1625delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16732902 | ||||||
| chr19:16733002
|
G | A | 4 | a0003c0003t0002g0065a0003c0003t0005g0141a0003c0003t0007g0064others(1): Show | 4 | HG02074.hp2 HG04184.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+1724G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733002 | ||||||
| chr19:16733026
|
G | A | 141 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(138): Show | 141 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.81+1748G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733026 | ||||||
| chr19:16733046
|
A | G | 53 | a0003c0003t0001g0210a0003c0003t0002g0127a0003c0003t0003g0143others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1768A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733046 | ||||||
| chr19:16733051
|
G | A | 64 | a0002c0001t0004g0032a0002c0001t0004g0034a0002c0001t0004g0035others(61): Show | 64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.81+1773G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733051 | ||||||
| chr19:16733146
|
A | C | 53 | a0003c0003t0001g0210a0003c0003t0002g0127a0003c0003t0003g0143others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+1868A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733146 | ||||||
| chr19:16733156
|
G | A | 60 | a0003c0003t0001g0210a0003c0003t0002g0127a0003c0003t0003g0143others(57): Show | 60 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.81+1878G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733156 | ||||||
| chr19:16733191
|
A | C | 144 | a0002c0001t0001g0164a0002c0001t0001g0260a0002c0001t0001g0261others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.81+1913A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733191 | ||||||
| chr19:16733192
|
G | A | 144 | a0002c0001t0001g0164a0002c0001t0001g0260a0002c0001t0001g0261others(141): Show | 144 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.81+1914G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733192 | ||||||
| chr19:16733280
|
G | A | 53 | a0003c0003t0001g0210a0003c0003t0002g0127a0003c0003t0003g0143others(50): Show | 53 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+2002G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733280 | ||||||
| chr19:16733291
|
C | T | 151 | a0002c0001t0001g0164a0002c0001t0001g0260a0002c0001t0001g0261others(148): Show | 151 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.81+2013C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733291 | ||||||
| chr19:16733326
|
G | C | 2 | a0004c0009t0005g0140a0004c0009t0005g0224 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.81+2048G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733326 | ||||||
| chr19:16733463
|
G | A | 1 | a0001c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.81+2185G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733463 | ||||||
| chr19:16733520
|
C | CA | 93 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0175others(90): Show | 93 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.81+2258dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16733520 | |||||
| chr19:16733520
|
CA | C | 143 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0153others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.81+2258delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16733520 | |||||
| chr19:16733749
|
C | G | 9 | a0001c0002t0020g0249a0002c0001t0001g0147a0006c0014t0008g0253others(6): Show | 9 | HG01099.hp2 HG02300.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+2471C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733749 | ||||||
| chr19:16733752
|
C | G | 9 | a0001c0002t0020g0249a0002c0001t0001g0147a0006c0014t0008g0253others(6): Show | 9 | HG01099.hp2 HG02300.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+2474C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733752 | ||||||
| chr19:16733792
|
C | T | 14 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(11): Show | 14 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+2514C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733792 | ||||||
| chr19:16733802
|
CG | C | 68 | a0001c0002t0020g0249a0002c0001t0001g0147a0003c0003t0001g0210others(65): Show | 68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.81+2526delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16733802 | |||||
| chr19:16733921
|
G | C | 9 | a0001c0002t0020g0249a0002c0001t0001g0147a0006c0014t0008g0253others(6): Show | 9 | HG01099.hp2 HG02300.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+2643G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733921 | ||||||
| chr19:16733931
|
A | G | 70 | a0001c0002t0020g0249a0002c0001t0001g0147a0003c0003t0001g0210others(67): Show | 70 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.81+2653A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733931 | ||||||
| chr19:16733962
|
C | G | 2 | a0006c0014t0008g0253a0006c0044t0001g0255 | 2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.82-2672C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16733962 | ||||||
| chr19:16734033
|
A | G | 73 | a0001c0002t0020g0249a0002c0001t0001g0147a0003c0003t0001g0210others(70): Show | 73 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.82-2601A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734033 | ||||||
| chr19:16734049
|
C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-2585C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734049 | ||||||
| chr19:16734140
|
G | A | 1 | a0003c0003t0007g0064 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.82-2494G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734140 | ||||||
| chr19:16734522
|
A | C | 60 | a0001c0002t0003g0144a0001c0002t0003g0163a0002c0001t0001g0164others(57): Show | 60 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-2112A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734522 | ||||||
| chr19:16734534
|
CA | C | 79 | a0001c0002t0003g0144a0001c0002t0003g0163a0002c0001t0001g0164others(76): Show | 79 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.82-2086delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734534 | |||||
| chr19:16734549
|
G | T | 2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.82-2085G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734549 | ||||||
| chr19:16734559
|
C | CT | 63 | a0001c0002t0020g0249a0002c0001t0001g0147a0003c0003t0001g0210others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.82-2064dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734559 | |||||
| chr19:16734608
|
G | A | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-2026G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734608 | ||||||
| chr19:16734612
|
T | C | 63 | a0001c0002t0020g0249a0002c0001t0001g0147a0003c0003t0001g0210others(60): Show | 63 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.82-2022T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734612 | ||||||
| chr19:16734652
|
C | A | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.82-1982C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734652 | ||||||
| chr19:16734734
|
C | CTATT | 18 | a0001c0002t0001g0196a0001c0002t0001g0218a0001c0002t0001g0291others(15): Show | 18 | HG00280.hp1 HG01081.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-1871_82-1868dup others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | |||||
| chr19:16734734
|
C | CTATTTAT others(1): Show |
38 | a0003c0003t0002g0127a0003c0003t0003g0143a0003c0003t0003g0288others(35): Show | 38 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-1875_82-1868dup others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | |||||
| chr19:16734734
|
C | CTATTTAT others(5): Show |
12 | a0004c0005t0006g0226a0004c0005t0006g0227a0004c0005t0006g0228others(9): Show | 12 | HG02258.hp2 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-1879_82-1868dup others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | |||||
| chr19:16734734
|
CTATTTAT others(1): Show |
C | 15 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(12): Show | 15 | HG01109.hp2 HG01167.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.82-1875_82-1868del others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | |||||
| chr19:16734734
|
CTATTTAT others(5): Show |
C | 1 | a0002c0007t0049g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.82-1879_82-1868del others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16734734 | |||||
| chr19:16734892
|
C | T | 2 | a0004c0005t0018g0256a0004c0009t0008g0286 | 2 | HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.82-1742C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734892 | ||||||
| chr19:16734929
|
C | A | 8 | a0001c0002t0001g0268a0001c0002t0001g0271a0001c0002t0003g0267others(5): Show | 8 | HG00738.hp1 HG01175.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-1705C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16734929 | ||||||
| chr19:16735114
|
G | A | 1 | a0016c0019t0008g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.82-1520G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735114 | ||||||
| chr19:16735164
|
G | A | 74 | a0001c0002t0003g0144a0001c0002t0003g0163a0002c0001t0001g0164others(71): Show | 74 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.82-1470G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735164 | ||||||
| chr19:16735256
|
C | T | 3 | a0005c0004t0002g0039a0005c0004t0003g0273a0040c0056t0001g0279 | 3 | HG01167.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.82-1378C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735256 | ||||||
| chr19:16735367
|
G | A | 9 | a0004c0005t0006g0225a0004c0009t0009g0047a0004c0060t0002g0125others(6): Show | 9 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-1267G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735367 | ||||||
| chr19:16735388
|
C | A | 1 | a0003c0006t0002g0082 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.82-1246C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735388 | ||||||
| chr19:16735399
|
G | A | 2 | a0003c0006t0001g0281a0003c0006t0001g0282 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.82-1235G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735399 | ||||||
| chr19:16735403
|
G | T | 1 | a0002c0001t0005g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.82-1231G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735403 | ||||||
| chr19:16735520
|
A | G | 4 | a0006c0015t0006g0293a0013c0018t0017g0294a0013c0018t0017g0295others(1): Show | 4 | HG02723.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-1114A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735520 | ||||||
| chr19:16735557
|
A | C | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.82-1077A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735557 | ||||||
| chr19:16735792
|
TGGAAGGA others(1): Show |
T | 72 | a0001c0002t0002g0063a0001c0002t0003g0144a0001c0002t0003g0163others(69): Show | 72 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.82-813_82-806delGG others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735792 | |||||
| chr19:16735795
|
AAGGAAGG others(64): Show |
A | 38 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(35): Show | 38 | HG01123.hp2 HG01167.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-806_82-736delAA others(69): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735795 | |||||
| chr19:16735803
|
AAGGAAGG others(56): Show |
A | 1 | a0004c0009t0013g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.82-805_82-743delAG others(61): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735803 | |||||
| chr19:16735807
|
AAGGAAGG others(52): Show |
A | 1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-805_82-747delAG others(57): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735807 | |||||
| chr19:16735811
|
AAGGAAGG others(48): Show |
A | 9 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(6): Show | 9 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-805_82-751delAG others(53): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735811 | |||||
| chr19:16735815
|
AAGGAAGG others(44): Show |
A | 16 | a0003c0003t0003g0288a0003c0006t0001g0281a0003c0006t0001g0282others(13): Show | 16 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.82-805_82-755delAG others(49): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735815 | |||||
| chr19:16735819
|
AAGGAAGG others(40): Show |
A | 1 | a0005c0004t0001g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.82-805_82-759delAG others(45): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735819 | |||||
| chr19:16735821
|
G | A | 3 | a0003c0003t0002g0066a0003c0006t0002g0061a0014c0054t0025g0118 | 3 | HG03209.hp1 HG03491.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.82-813G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735821 | ||||||
| chr19:16735829
|
A | AGAAG | 4 | a0001c0002t0001g0199a0002c0001t0005g0241a0002c0007t0001g0239others(1): Show | 4 | NA18951.hp1 NA18960.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-770_82-767dupAG others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735829 | |||||
| chr19:16735829
|
A | G | 22 | a0003c0003t0002g0066a0003c0006t0002g0061a0004c0005t0006g0225others(19): Show | 22 | HG01109.hp2 HG01361.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.82-805A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735829 | ||||||
| chr19:16735829
|
AGAAG | A | 17 | a0001c0002t0001g0291a0001c0002t0004g0033a0002c0001t0001g0137others(14): Show | 17 | HG00735.hp1 HG00735.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.82-770_82-767delAG others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735829 | |||||
| chr19:16735833
|
G | A | 10 | a0006c0014t0002g0015a0006c0014t0009g0014a0006c0014t0009g0016others(7): Show | 10 | HG01109.hp2 HG01361.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-801G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735833 | ||||||
| chr19:16735837
|
G | A | 3 | a0004c0005t0006g0225a0004c0060t0002g0125a0043c0064t0002g0300 | 3 | HG02886.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82-797G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735837 | ||||||
| chr19:16735841
|
G | A | 6 | a0004c0009t0009g0047a0008c0010t0010g0131a0008c0010t0047g0005others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-793G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735841 | ||||||
| chr19:16735843
|
AAGGAAGG others(16): Show |
A | 1 | a0004c0005t0006g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82-766_82-744delGG others(21): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735843 | |||||
| chr19:16735847
|
AAGGAAGG others(12): Show |
A | 2 | a0008c0010t0010g0131a0046c0062t0030g0250 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.82-766_82-748delGG others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735847 | |||||
| chr19:16735850
|
GAAGGA | G | 3 | a0003c0003t0002g0066a0003c0006t0002g0061a0014c0054t0025g0118 | 3 | HG03209.hp1 HG03491.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.82-782_82-778delAG others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735850 | |||||
| chr19:16735854
|
GAAGGA | G | 7 | a0004c0005t0048g0002a0009c0029t0002g0297a0009c0029t0002g0298others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-778_82-774delAG others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735854 | |||||
| chr19:16735858
|
GA | G | 63 | a0001c0002t0003g0144a0001c0002t0003g0163a0002c0001t0001g0164others(60): Show | 63 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.82-774delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735858 | |||||
| chr19:16735858
|
GAAGGAAG others(5): Show |
G | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-774_82-763delAG others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735858 | |||||
| chr19:16735863
|
AAGG | A | 74 | a0001c0002t0003g0144a0001c0002t0003g0163a0002c0001t0001g0164others(71): Show | 74 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.82-766_82-764delGG others(1): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735863 | |||||
| chr19:16735864
|
A | G | 1 | a0005c0004t0002g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.82-770A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735864 | ||||||
| chr19:16735866
|
G | A | 1 | a0005c0004t0002g0103 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.82-768G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735866 | ||||||
| chr19:16735866
|
G | GA | 4 | a0002c0001t0005g0169a0004c0060t0002g0125a0008c0010t0047g0005others(1): Show | 4 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-767dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735866 | |||||
| chr19:16735866
|
GAGGA | G | 5 | a0004c0005t0001g0296a0006c0015t0006g0290a0006c0015t0041g0053others(2): Show | 5 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-739_82-736delAG others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735866 | |||||
| chr19:16735868
|
G | A | 7 | a0006c0014t0002g0015a0006c0014t0009g0014a0006c0014t0009g0016others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-766G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735868 | ||||||
| chr19:16735870
|
A | G | 7 | a0006c0014t0002g0015a0006c0014t0009g0014a0006c0014t0009g0016others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-764A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735870 | ||||||
| chr19:16735960
|
A | T | 20 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(17): Show | 20 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-674A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16735960 | ||||||
| chr19:16735963
|
C | CA | 27 | a0001c0002t0020g0249a0002c0001t0001g0147a0002c0001t0001g0242others(24): Show | 27 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.82-656dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735963 | |||||
| chr19:16735963
|
C | CAA | 62 | a0001c0002t0003g0163a0002c0001t0001g0164a0002c0001t0001g0197others(59): Show | 62 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.82-657_82-656dupAA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735963 | |||||
| chr19:16735963
|
CA | C | 11 | a0001c0008t0027g0136a0002c0001t0001g0260a0004c0005t0006g0226others(8): Show | 11 | HG02027.hp1 HG02258.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-656delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16735963 | |||||
| chr19:16736082
|
C | T | 6 | a0004c0009t0009g0047a0004c0060t0002g0125a0008c0010t0047g0005others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-552C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736082 | ||||||
| chr19:16736189
|
C | CTTCGTTC others(21): Show |
3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.82-442_82-441insGT others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736189 | |||||
| chr19:16736193
|
T | C | 4 | a0001c0008t0001g0139a0004c0005t0006g0225a0008c0010t0010g0131others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-441T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736193 | ||||||
| chr19:16736193
|
T | TTTCCTTC others(29): Show |
1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-434_82-433insTT others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(33): Show |
2 | a0017c0021t0002g0051a0043c0064t0002g0300 | 2 | HG02723.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82-434_82-433insTT others(38): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(37): Show |
1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.82-434_82-433insTT others(42): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(41): Show |
2 | a0004c0009t0009g0047a0017c0021t0002g0046 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.82-434_82-433insTT others(46): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(13): Show |
1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-434_82-433insTT others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(21): Show |
3 | a0019c0024t0001g0251a0021c0026t0002g0083a0033c0052t0001g0254 | 3 | HG02293.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.82-434_82-433insTT others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(25): Show |
5 | a0001c0002t0020g0249a0006c0014t0008g0253a0006c0044t0001g0255others(2): Show | 5 | HG01099.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-434_82-433insTT others(30): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(29): Show |
1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.82-434_82-433insTT others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736193
|
T | TTTCCTTC others(33): Show |
1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.82-434_82-433insTT others(38): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736193 | |||||
| chr19:16736209
|
T | C | 21 | a0001c0002t0020g0249a0001c0008t0001g0139a0002c0001t0001g0147others(18): Show | 21 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(18): Show |
intron_variant | MODIFIER | c.82-425T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736209 | ||||||
| chr19:16736209
|
T | TTTCCTTC others(5): Show |
134 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.82-419_82-408dupTC others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(9): Show |
3 | a0002c0001t0001g0160a0002c0007t0001g0221a0006c0015t0028g0204 | 3 | HG00639.hp1 HG01109.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.82-423_82-408dupTC others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(13): Show |
4 | a0006c0014t0002g0015a0006c0014t0009g0014a0006c0014t0009g0016others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(17): Show |
10 | a0004c0005t0006g0226a0004c0005t0006g0227a0004c0005t0006g0228others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(21): Show |
56 | a0001c0002t0003g0144a0001c0002t0003g0163a0002c0001t0001g0164others(53): Show | 56 | HG00609.hp1 HG00642.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(25): Show |
39 | a0002c0001t0001g0197a0002c0001t0004g0032a0002c0001t0004g0034others(36): Show | 39 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(30): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(29): Show |
23 | a0003c0003t0002g0091a0003c0003t0003g0288a0003c0003t0007g0064others(20): Show | 23 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(33): Show |
5 | a0003c0003t0002g0065a0004c0009t0008g0286a0005c0016t0002g0056others(2): Show | 5 | HG02735.hp1 HG02886.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-408_82-407insTC others(38): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(37): Show |
2 | a0004c0005t0048g0002a0005c0004t0002g0039 | 2 | HG01167.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.82-408_82-407insTC others(42): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(41): Show |
1 | a0003c0006t0001g0281 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.82-408_82-407insTC others(46): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736209
|
T | TTTCCTTC others(45): Show |
1 | a0003c0006t0001g0282 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.82-408_82-407insTC others(50): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16736209 | |||||
| chr19:16736227
|
A | T | 20 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(17): Show | 20 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-407A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736227 | ||||||
| chr19:16736267
|
C | G | 1 | a0007c0012t0001g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.82-367C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736267 | ||||||
| chr19:16736364
|
G | T | 10 | a0003c0003t0002g0117a0009c0028t0002g0115a0009c0028t0034g0258others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-270G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736364 | ||||||
| chr19:16736376
|
C | A | 1 | a0011c0011t0001g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.82-258C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736376 | ||||||
| chr19:16736431
|
C | G | 4 | a0002c0001t0001g0159a0002c0001t0020g0289a0002c0007t0001g0040others(1): Show | 4 | HG00099.hp1 HG01074.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-203C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736431 | ||||||
| chr19:16736495
|
C | A | 9 | a0004c0005t0006g0225a0004c0009t0009g0047a0004c0060t0002g0125others(6): Show | 9 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-139C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 3/18 | chr19 | 16736495 | ||||||
| chr19:16736955
|
G | A | 1 | a0026c0040t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.198+205G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16736955 | ||||||
| chr19:16737054
|
T | G | 4 | a0012c0017t0002g0018a0012c0017t0002g0019a0041c0065t0032g0166others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+304T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737054 | ||||||
| chr19:16737176
|
C | T | 3 | a0003c0003t0004g0079a0005c0004t0002g0074a0005c0004t0002g0103 | 3 | HG00558.hp2 HG02015.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.198+426C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737176 | ||||||
| chr19:16737566
|
G | GT | 14 | a0001c0002t0020g0249a0002c0001t0005g0246a0004c0005t0039g0084others(11): Show | 14 | HG01081.hp1 HG01099.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+831dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737566 | |||||
| chr19:16737567
|
T | G | 6 | a0004c0009t0009g0047a0004c0060t0002g0125a0008c0010t0047g0005others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+817T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737567 | ||||||
| chr19:16737568
|
T | G | 3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+818T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737568 | ||||||
| chr19:16737577
|
T | C | 3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+827T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737577 | ||||||
| chr19:16737635
|
C | T | 1 | a0039c0057t0026g0202 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+885C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737635 | ||||||
| chr19:16737699
|
C | T | 2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.198+949C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737699 | ||||||
| chr19:16737817
|
T | C | 2 | a0002c0007t0002g0122a0035c0050t0007g0104 | 2 | HG02132.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.198+1067T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737817 | ||||||
| chr19:16737943
|
C | T | 6 | a0004c0005t0006g0226a0004c0005t0006g0227a0004c0005t0006g0228others(3): Show | 6 | HG02258.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+1193C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737943 | ||||||
| chr19:16737954
|
G | A | 2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.198+1204G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737954 | ||||||
| chr19:16737964
|
C | CAAAA | 3 | a0002c0001t0001g0147a0004c0005t0039g0084a0021c0026t0002g0083 | 3 | HG01081.hp1 HG02293.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.198+1214_198+1215i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CAAAAGAA others(132): Show |
1 | a0019c0024t0001g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(141): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CAAAAGAA others(157): Show |
1 | a0019c0024t0001g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(166): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CAAAAGAA others(162): Show |
1 | a0006c0044t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.198+1214_198+1215i others(171): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CAAAAGAA others(172): Show |
1 | a0033c0052t0001g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(181): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CAAAAGAA others(182): Show |
1 | a0006c0014t0008g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(191): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CAAAAGAA others(187): Show |
1 | a0001c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(196): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CAAAAGAA others(142): Show |
1 | a0032c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.198+1214_198+1215i others(151): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16737964 | ||||||
| chr19:16737964
|
C | CGAAAA | 88 | a0001c0002t0001g0146a0001c0002t0001g0199a0001c0002t0001g0268others(85): Show | 88 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.198+1259_198+1263d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
C | CGAAAAGA others(3): Show |
52 | a0001c0002t0001g0170a0002c0001t0001g0260a0002c0001t0001g0261others(49): Show | 52 | HG00544.hp1 HG00642.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.198+1254_198+1263d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
C | CGAAAAGA others(8): Show |
7 | a0003c0003t0002g0006a0003c0003t0002g0067a0003c0003t0002g0068others(4): Show | 7 | HG01361.hp1 HG02056.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+1249_198+1263d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
C | CGAAAAGA others(13): Show |
6 | a0004c0005t0029g0265a0004c0060t0002g0125a0017c0021t0002g0051others(3): Show | 6 | HG02615.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+1244_198+1263d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
C | CGAAAAGA others(18): Show |
2 | a0008c0010t0010g0131a0034c0051t0002g0028 | 2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.198+1239_198+1263d others(27): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
C | CGAAAAGA others(23): Show |
1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.198+1234_198+1263d others(32): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
CGAAAA | C | 9 | a0006c0014t0002g0015a0006c0014t0009g0014a0006c0014t0009g0016others(6): Show | 9 | HG01109.hp2 HG02109.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1259_198+1263d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
CGAAAAGA others(3): Show |
C | 3 | a0001c0002t0001g0193a0001c0002t0005g0192a0024c0036t0001g0209 | 3 | HG02293.hp2 NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.198+1254_198+1263d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16737964
|
CGAAAAGA others(13): Show |
C | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.198+1244_198+1263d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16737964 | |||||
| chr19:16738003
|
A | AAG | 7 | a0001c0002t0020g0249a0006c0014t0008g0253a0006c0044t0001g0255others(4): Show | 7 | HG01099.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+1255_198+1256d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | |||||
| chr19:16738003
|
A | AAGAAAAG others(98): Show |
1 | a0021c0026t0002g0083 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.198+1263_198+1264i others(107): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | |||||
| chr19:16738003
|
A | AAGAAAAG others(122): Show |
1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.198+1263_198+1264i others(131): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | |||||
| chr19:16738003
|
A | AAGAAAAG others(123): Show |
1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.198+1263_198+1264i others(132): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738003 | |||||
| chr19:16738178
|
C | A | 3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+1428C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738178 | ||||||
| chr19:16738216
|
C | T | 1 | a0001c0002t0001g0291 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.198+1466C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738216 | ||||||
| chr19:16738391
|
AAACCCCA others(472): Show |
A | 1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.198+1644_198+2122d others(2): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738391 | |||||
| chr19:16738396
|
C | G | 2 | a0016c0019t0016g0003a0016c0019t0016g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.198+1646C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738396 | ||||||
| chr19:16738429
|
C | T | 8 | a0004c0005t0001g0296a0006c0015t0006g0290a0006c0015t0006g0293others(5): Show | 8 | HG02055.hp1 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+1679C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738429 | ||||||
| chr19:16738448
|
G | A | 161 | a0001c0002t0003g0144a0001c0002t0003g0163a0001c0002t0020g0249others(158): Show | 161 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.198+1698G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738448 | ||||||
| chr19:16738555
|
G | A | 1 | a0025c0034t0001g0133 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.198+1805G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738555 | ||||||
| chr19:16738566
|
C | CA | 23 | a0001c0002t0001g0142a0001c0002t0001g0189a0001c0002t0012g0178others(20): Show | 23 | HG00609.hp1 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+1834dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738566 | |||||
| chr19:16738566
|
C | CAA | 14 | a0004c0005t0006g0225a0004c0009t0009g0047a0004c0060t0002g0125others(11): Show | 14 | HG02451.hp2 HG02615.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+1833_198+1834d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738566 | |||||
| chr19:16738566
|
CA | C | 56 | a0001c0002t0001g0193a0002c0001t0001g0260a0002c0001t0001g0261others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.198+1834delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738566 | |||||
| chr19:16738627
|
TA | T | 19 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(16): Show | 19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1878delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738627 | ||||||
| chr19:16738629
|
T | G | 19 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(16): Show | 19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1879T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738629 | ||||||
| chr19:16738630
|
T | C | 19 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(16): Show | 19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1880T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738630 | ||||||
| chr19:16738730
|
C | A | 19 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(16): Show | 19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+1980C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738730 | ||||||
| chr19:16738748
|
T | A | 1 | a0001c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.198+1998T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738748 | ||||||
| chr19:16738748
|
TTA | T | 6 | a0004c0009t0009g0047a0004c0060t0002g0125a0008c0010t0047g0005others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+2009_198+2010d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738748 | |||||
| chr19:16738749
|
T | A | 3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+1999T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738749 | ||||||
| chr19:16738750
|
A | ATATATAT others(2): Show |
3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+2001_198+2009d others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738750 | |||||
| chr19:16738768
|
G | A | 1 | a0003c0003t0004g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.198+2018G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738768 | ||||||
| chr19:16738768
|
G | T | 1 | a0009c0029t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198+2018G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738768 | ||||||
| chr19:16738768
|
GATATATA | G | 10 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(7): Show | 10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+2036_198+2042d others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738768 | |||||
| chr19:16738768
|
GATATATA others(7): Show |
G | 72 | a0002c0001t0001g0160a0002c0001t0001g0164a0002c0001t0001g0197others(69): Show | 72 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.198+2029_198+2042d others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738768 | |||||
| chr19:16738782
|
A | ATATTATA others(16): Show |
1 | a0009c0029t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198+2032_198+2033i others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738782 | ||||||
| chr19:16738782
|
A | G | 1 | a0003c0003t0004g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.198+2032A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738782 | ||||||
| chr19:16738802
|
ATAC | A | 10 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(7): Show | 10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+2055_198+2057d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738802 | |||||
| chr19:16738805
|
C | T | 7 | a0004c0005t0006g0225a0004c0009t0009g0047a0004c0060t0002g0125others(4): Show | 7 | HG02723.hp2 HG02886.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+2055C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738805 | ||||||
| chr19:16738822
|
T | C | 1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.198+2072T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738822 | ||||||
| chr19:16738829
|
T | TATACATT others(277): Show |
1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.198+2092_198+2093i others(286): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | |||||
| chr19:16738829
|
T | TATACATT others(77): Show |
4 | a0004c0009t0009g0047a0017c0021t0002g0046a0017c0021t0002g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+2092_198+2093i others(86): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | |||||
| chr19:16738829
|
T | TATACATT others(119): Show |
2 | a0004c0060t0002g0125a0008c0010t0047g0005 | 2 | HG02886.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.198+2092_198+2093i others(128): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | |||||
| chr19:16738829
|
T | TATACATT others(319): Show |
3 | a0006c0014t0008g0253a0006c0044t0001g0255a0032c0053t0001g0252 | 3 | HG02451.hp2 HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198+2106_198+2107i others(328): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | |||||
| chr19:16738829
|
T | TATACATT others(298): Show |
5 | a0004c0005t0039g0084a0019c0024t0001g0251a0019c0024t0001g0259others(2): Show | 5 | HG01081.hp1 HG02293.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+2106_198+2107i others(307): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | |||||
| chr19:16738829
|
T | TATACATT others(340): Show |
1 | a0001c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.198+2106_198+2107i others(349): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738829 | |||||
| chr19:16738843
|
T | A | 7 | a0004c0005t0006g0225a0004c0009t0009g0047a0008c0010t0010g0131others(4): Show | 7 | HG02615.hp2 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+2093T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738843 | ||||||
| chr19:16738847
|
T | G | 12 | a0004c0005t0001g0296a0006c0014t0002g0015a0006c0014t0009g0014others(9): Show | 12 | HG01109.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+2097T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738847 | ||||||
| chr19:16738860
|
C | A | 19 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(16): Show | 19 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+2110C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738860 | ||||||
| chr19:16738886
|
A | ATATATAA others(56): Show |
3 | a0004c0005t0006g0225a0008c0010t0010g0131a0046c0062t0030g0250 | 3 | HG02615.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.198+2142_198+2143i others(65): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16738886 | |||||
| chr19:16738913
|
C | T | 20 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0006g0225others(17): Show | 20 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(17): Show |
intron_variant | MODIFIER | c.198+2163C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16738913 | ||||||
| chr19:16739189
|
A | G | 9 | a0002c0001t0003g0195a0002c0001t0004g0107a0002c0001t0004g0108others(6): Show | 9 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+2439A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739189 | ||||||
| chr19:16739190
|
G | GA | 162 | a0001c0002t0020g0249a0002c0001t0001g0147a0002c0001t0001g0160others(159): Show | 162 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.198+2451dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739190 | |||||
| chr19:16739242
|
C | T | 1 | a0005c0016t0002g0081 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.198+2492C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739242 | ||||||
| chr19:16739272
|
A | T | 2 | a0008c0010t0010g0276a0008c0010t0010g0284 | 2 | HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.198+2522A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739272 | ||||||
| chr19:16739284
|
G | A | 11 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(8): Show | 11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+2534G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739284 | ||||||
| chr19:16739329
|
C | CA | 24 | a0001c0002t0001g0142a0001c0002t0001g0170a0001c0002t0001g0179others(21): Show | 24 | HG00735.hp2 HG01175.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.198+2605dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | |||||
| chr19:16739329
|
CA | C | 33 | a0001c0002t0001g0196a0001c0002t0001g0291a0001c0002t0002g0007others(30): Show | 33 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+2605delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | |||||
| chr19:16739329
|
CAA | C | 70 | a0002c0001t0001g0160a0002c0001t0001g0197a0002c0001t0003g0162others(67): Show | 70 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.198+2604_198+2605d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | |||||
| chr19:16739329
|
CAAA | C | 51 | a0002c0001t0001g0164a0002c0001t0001g0260a0002c0001t0001g0261others(48): Show | 51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.198+2603_198+2605d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | |||||
| chr19:16739329
|
CAAAA | C | 13 | a0004c0005t0001g0296a0004c0005t0018g0256a0005c0004t0002g0039others(10): Show | 13 | HG01109.hp2 HG01167.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.198+2602_198+2605d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16739329 | |||||
| chr19:16739355
|
A | T | 5 | a0004c0009t0009g0047a0017c0021t0002g0046a0017c0021t0002g0051others(2): Show | 5 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+2605A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739355 | ||||||
| chr19:16739377
|
G | A | 1 | a0001c0002t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.198+2627G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739377 | ||||||
| chr19:16739388
|
G | A | 1 | a0003c0003t0002g0085 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+2638G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739388 | ||||||
| chr19:16739486
|
G | A | 1 | a0011c0011t0011g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198+2736G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739486 | ||||||
| chr19:16739705
|
T | C | 1 | a0009c0069t0043g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+2955T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739705 | ||||||
| chr19:16739724
|
T | C | 11 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(8): Show | 11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.198+2974T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739724 | ||||||
| chr19:16739922
|
A | G | 162 | a0001c0002t0020g0249a0002c0001t0001g0147a0002c0001t0001g0160others(159): Show | 162 | HG00280.hp1 HG00323.hp1 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.198+3172A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739922 | ||||||
| chr19:16739949
|
G | A | 1 | a0040c0056t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.198+3199G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16739949 | ||||||
| chr19:16740026
|
T | G | 17 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(14): Show | 17 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+3276T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740026 | ||||||
| chr19:16740193
|
G | A | 17 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(14): Show | 17 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+3443G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740193 | ||||||
| chr19:16740220
|
G | A | 2 | a0003c0006t0001g0281a0003c0006t0001g0282 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.198+3470G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740220 | ||||||
| chr19:16740398
|
A | C | 108 | a0001c0002t0003g0144a0001c0002t0003g0163a0001c0002t0020g0249others(105): Show | 108 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.198+3648A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740398 | ||||||
| chr19:16740642
|
A | AT | 13 | a0001c0002t0001g0218a0002c0001t0002g0029a0002c0001t0003g0162others(10): Show | 13 | HG00609.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.199-3757dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16740642 | |||||
| chr19:16740642
|
A | ATTTTTTT | 6 | a0004c0009t0009g0047a0004c0060t0002g0125a0008c0010t0047g0005others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-3763_199-3757d others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16740642 | |||||
| chr19:16740642
|
ATTTTTT | A | 11 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(8): Show | 11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-3762_199-3757d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16740642 | |||||
| chr19:16740680
|
C | A | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.199-3741C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740680 | ||||||
| chr19:16740934
|
G | A | 3 | a0001c0002t0002g0031a0001c0002t0007g0030a0001c0002t0011g0105 | 3 | HG02015.hp1 NA18951.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.199-3487G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16740934 | ||||||
| chr19:16741037
|
A | G | 11 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(8): Show | 11 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-3384A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741037 | ||||||
| chr19:16741104
|
G | A | 10 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(7): Show | 10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-3317G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741104 | ||||||
| chr19:16741123
|
A | G | 15 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(12): Show | 15 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-3298A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741123 | ||||||
| chr19:16741301
|
T | G | 1 | a0017c0021t0002g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.199-3120T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741301 | ||||||
| chr19:16741366
|
G | GTGT | 10 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(7): Show | 10 | HG01081.hp1 HG01099.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-3053_199-3051d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741366 | |||||
| chr19:16741368
|
G | GT | 12 | a0001c0002t0002g0063a0001c0002t0005g0192a0002c0001t0003g0195others(9): Show | 12 | HG01123.hp1 HG01943.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-3036dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741368 | |||||
| chr19:16741368
|
GT | G | 84 | a0002c0001t0001g0164a0002c0001t0001g0197a0002c0001t0001g0260others(81): Show | 84 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.199-3036delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741368 | |||||
| chr19:16741436
|
G | A | 4 | a0004c0009t0009g0047a0017c0021t0002g0046a0017c0021t0002g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-2985G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741436 | ||||||
| chr19:16741439
|
C | T | 1 | a0037c0045t0016g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.199-2982C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741439 | ||||||
| chr19:16741478
|
T | TCCTCAGC others(2315): Show |
1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199-1500_199-1499i others(2324): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16741478 | |||||
| chr19:16741565
|
C | T | 4 | a0006c0014t0002g0015a0006c0014t0009g0014a0006c0014t0009g0016others(1): Show | 4 | HG01109.hp2 HG02109.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2856C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741565 | ||||||
| chr19:16741968
|
G | A | 1 | a0003c0003t0002g0117 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.199-2453G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16741968 | ||||||
| chr19:16742046
|
G | T | 12 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(9): Show | 12 | HG01081.hp1 HG01099.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-2375G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742046 | ||||||
| chr19:16742227
|
T | A | 2 | a0009c0029t0002g0297a0009c0029t0002g0298 | 2 | HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.199-2194T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742227 | ||||||
| chr19:16742272
|
G | A | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-2149G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742272 | ||||||
| chr19:16742353
|
C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-2068C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742353 | ||||||
| chr19:16742393
|
A | C | 1 | a0003c0003t0002g0006 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.199-2028A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742393 | ||||||
| chr19:16742452
|
C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-1969C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742452 | ||||||
| chr19:16742511
|
C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-1910C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742511 | ||||||
| chr19:16742568
|
AG | A | 6 | a0001c0002t0020g0249a0002c0001t0001g0147a0004c0005t0039g0084others(3): Show | 6 | HG01081.hp1 HG01099.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-1850delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742568 | |||||
| chr19:16742635
|
C | A | 4 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(1): Show | 4 | HG01167.hp1 HG01884.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1786C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742635 | ||||||
| chr19:16742707
|
G | A | 9 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(6): Show | 9 | HG01167.hp1 HG01884.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-1714G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742707 | ||||||
| chr19:16742730
|
G | A | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.199-1691G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742730 | ||||||
| chr19:16742731
|
C | T | 5 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(2): Show | 5 | HG01167.hp1 HG01884.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-1690C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742731 | ||||||
| chr19:16742847
|
A | T | 4 | a0004c0009t0009g0047a0017c0021t0002g0046a0017c0021t0002g0051others(1): Show | 4 | HG02723.hp2 HG03471.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1574A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742847 | ||||||
| chr19:16742848
|
A | T | 6 | a0004c0009t0009g0047a0004c0060t0002g0125a0017c0021t0002g0046others(3): Show | 6 | HG02723.hp2 HG02886.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-1573A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16742848 | ||||||
| chr19:16742881
|
C | CTAT | 44 | a0001c0002t0003g0163a0001c0002t0004g0009a0001c0002t0007g0030others(41): Show | 44 | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.199-1499_199-1497d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | |||||
| chr19:16742881
|
C | CTATTAT | 3 | a0002c0001t0004g0034a0002c0001t0005g0169a0017c0021t0001g0231 | 3 | HG01884.hp2 HG03688.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.199-1502_199-1497d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | |||||
| chr19:16742881
|
CTAT | C | 85 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(82): Show | 85 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.199-1499_199-1497d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | |||||
| chr19:16742881
|
CTATTAT | C | 23 | a0001c0002t0001g0157a0001c0002t0001g0165a0001c0002t0001g0191others(20): Show | 23 | HG00099.hp2 HG00609.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.199-1502_199-1497d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | |||||
| chr19:16742881
|
CTATTATT others(2): Show |
C | 4 | a0002c0001t0001g0260a0008c0010t0010g0276a0008c0010t0010g0278others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1505_199-1497d others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | |||||
| chr19:16742881
|
CTATTATT others(5): Show |
C | 1 | a0002c0001t0001g0160 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.199-1508_199-1497d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | |||||
| chr19:16742881
|
CTATTATT others(8): Show |
C | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-1511_199-1497d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16742881 | |||||
| chr19:16743057
|
T | C | 4 | a0006c0014t0008g0253a0006c0044t0001g0255a0011c0011t0011g0017others(1): Show | 4 | HG02109.hp1 HG02965.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-1364T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743057 | ||||||
| chr19:16743071
|
C | T | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.199-1350C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743071 | ||||||
| chr19:16743109
|
T | C | 12 | a0001c0035t0002g0020a0002c0001t0001g0147a0004c0005t0039g0084others(9): Show | 12 | HG01081.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-1312T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743109 | ||||||
| chr19:16743195
|
G | A | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.199-1226G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743195 | ||||||
| chr19:16743273
|
C | T | 3 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262 | 3 | HG01167.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-1148C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743273 | ||||||
| chr19:16743296
|
G | A | 1 | a0001c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.199-1125G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743296 | ||||||
| chr19:16743478
|
G | C | 7 | a0010c0013t0008g0194a0010c0013t0009g0045a0010c0013t0013g0172others(4): Show | 7 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-943G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743478 | ||||||
| chr19:16743648
|
C | CCATA | 3 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262 | 3 | HG01167.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-768_199-765dup others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16743648 | |||||
| chr19:16743668
|
A | G | 10 | a0004c0005t0001g0296a0009c0028t0002g0115a0009c0028t0034g0258others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-753A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743668 | ||||||
| chr19:16743672
|
A | G | 16 | a0004c0005t0001g0296a0004c0009t0008g0286a0004c0009t0013g0206others(13): Show | 16 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-749A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743672 | ||||||
| chr19:16743675
|
A | T | 188 | a0001c0002t0003g0186a0002c0001t0001g0137a0002c0001t0001g0147others(185): Show | 188 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.199-746A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743675 | ||||||
| chr19:16743676
|
G | A | 1 | a0003c0003t0002g0085 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199-745G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743676 | ||||||
| chr19:16743680
|
G | A | 10 | a0004c0005t0001g0296a0009c0028t0002g0115a0009c0028t0034g0258others(7): Show | 10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-741G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743680 | ||||||
| chr19:16743680
|
G | GTTTGTTT others(1): Show |
44 | a0002c0001t0001g0147a0004c0005t0006g0211a0004c0005t0006g0225others(41): Show | 44 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.199-738_199-737ins others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16743680 | |||||
| chr19:16743775
|
C | T | 75 | a0002c0001t0001g0159a0002c0001t0001g0160a0002c0001t0001g0164others(72): Show | 75 | HG00099.hp1 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.199-646C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743775 | ||||||
| chr19:16743792
|
C | T | 1 | a0003c0003t0002g0006 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.199-629C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743792 | ||||||
| chr19:16743839
|
C | T | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.199-582C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743839 | ||||||
| chr19:16743881
|
C | T | 5 | a0002c0001t0001g0147a0004c0005t0039g0084a0006c0014t0008g0253others(2): Show | 5 | HG01081.hp1 HG02280.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-540C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743881 | ||||||
| chr19:16743929
|
C | T | 54 | a0002c0001t0001g0147a0004c0005t0001g0296a0004c0005t0006g0211others(51): Show | 54 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.199-492C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743929 | ||||||
| chr19:16743945
|
A | T | 5 | a0004c0005t0018g0256a0004c0005t0029g0265a0004c0009t0008g0205others(2): Show | 5 | HG02258.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-476A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16743945 | ||||||
| chr19:16744050
|
A | G | 1 | a0002c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.199-371A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744050 | ||||||
| chr19:16744089
|
G | C | 55 | a0002c0001t0001g0147a0004c0005t0001g0296a0004c0005t0006g0211others(52): Show | 55 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.199-332G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744089 | ||||||
| chr19:16744130
|
A | T | 54 | a0002c0001t0001g0147a0004c0005t0001g0296a0004c0005t0006g0211others(51): Show | 54 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.199-291A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744130 | ||||||
| chr19:16744138
|
C | A | 1 | a0005c0004t0003g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.199-283C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744138 | ||||||
| chr19:16744316
|
G | T | 3 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262 | 3 | HG01167.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-105G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 4/18 | chr19 | 16744316 | ||||||
| chr19:16744780
|
C | T | 1 | a0009c0029t0002g0298 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.496+62C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16744780 | ||||||
| chr19:16744983
|
C | A | 1 | a0033c0052t0001g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.496+265C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16744983 | ||||||
| chr19:16745067
|
A | G | 1 | a0009c0028t0034g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.496+349A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745067 | ||||||
| chr19:16745179
|
A | G | 74 | a0001c0002t0001g0146a0001c0002t0001g0199a0001c0002t0001g0208others(71): Show | 74 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.496+461A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745179 | ||||||
| chr19:16745204
|
T | C | 126 | a0001c0002t0001g0146a0001c0002t0012g0203a0001c0008t0001g0134others(123): Show | 126 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.496+486T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745204 | ||||||
| chr19:16745225
|
A | G | 21 | a0002c0001t0001g0260a0002c0001t0001g0261a0002c0001t0001g0262others(18): Show | 21 | HG01109.hp2 HG01167.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.496+507A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745225 | ||||||
| chr19:16745294
|
G | A | 1 | a0001c0031t0001g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.496+576G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745294 | ||||||
| chr19:16745342
|
C | T | 1 | a0002c0007t0002g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.496+624C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745342 | ||||||
| chr19:16745358
|
G | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.496+640G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745358 | ||||||
| chr19:16745375
|
C | T | 60 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(57): Show | 60 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.496+657C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745375 | ||||||
| chr19:16745481
|
A | C | 200 | a0001c0002t0001g0181a0001c0002t0002g0007a0001c0002t0002g0123others(197): Show | 200 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.496+763A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745481 | ||||||
| chr19:16745485
|
T | G | 9 | a0001c0035t0002g0020a0004c0005t0006g0226a0009c0068t0040g0116others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+767T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745485 | ||||||
| chr19:16745508
|
C | T | 18 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(15): Show | 18 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.496+790C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745508 | ||||||
| chr19:16745565
|
C | CA | 16 | a0001c0002t0002g0007a0002c0001t0001g0147a0002c0001t0014g0187others(13): Show | 16 | HG01433.hp2 HG01516.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.496+862dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16745565 | |||||
| chr19:16745573
|
A | T | 8 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+855A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745573 | ||||||
| chr19:16745679
|
G | A | 8 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+961G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745679 | ||||||
| chr19:16745776
|
G | A | 1 | a0002c0001t0003g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.496+1058G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745776 | ||||||
| chr19:16745904
|
G | A | 29 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(26): Show | 29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1186G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745904 | ||||||
| chr19:16745909
|
C | T | 1 | a0006c0044t0001g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.496+1191C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745909 | ||||||
| chr19:16745930
|
T | A | 2 | a0006c0015t0028g0204a0014c0054t0025g0118 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.496+1212T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16745930 | ||||||
| chr19:16746036
|
C | G | 1 | a0007c0067t0003g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.496+1318C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746036 | ||||||
| chr19:16746043
|
A | G | 2 | a0003c0003t0004g0073a0003c0003t0004g0079 | 2 | HG02015.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.496+1325A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746043 | ||||||
| chr19:16746053
|
C | T | 41 | a0003c0006t0002g0100a0004c0005t0029g0265a0004c0005t0048g0002others(38): Show | 41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.496+1335C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746053 | ||||||
| chr19:16746145
|
C | T | 87 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(84): Show | 87 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.496+1427C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746145 | ||||||
| chr19:16746154
|
G | T | 2 | a0007c0012t0001g0234a0007c0012t0001g0235 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.496+1436G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746154 | ||||||
| chr19:16746189
|
AT | A | 19 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(16): Show | 19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+1474delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16746189 | |||||
| chr19:16746192
|
TA | T | 22 | a0001c0002t0003g0163a0002c0001t0003g0195a0002c0001t0005g0246others(19): Show | 22 | HG01496.hp1 HG01516.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.496+1486delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16746192 | |||||
| chr19:16746263
|
C | G | 8 | a0003c0006t0002g0100a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1545C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746263 | ||||||
| chr19:16746264
|
G | A | 1 | a0002c0007t0001g0239 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.496+1546G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746264 | ||||||
| chr19:16746278
|
T | C | 6 | a0004c0005t0001g0296a0006c0044t0001g0255a0017c0021t0001g0231others(3): Show | 6 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+1560T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746278 | ||||||
| chr19:16746296
|
A | G | 8 | a0003c0006t0002g0100a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1578A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746296 | ||||||
| chr19:16746449
|
C | T | 8 | a0003c0006t0002g0100a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1731C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746449 | ||||||
| chr19:16746548
|
C | T | 1 | a0001c0002t0001g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.496+1830C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746548 | ||||||
| chr19:16746565
|
C | T | 62 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(59): Show | 62 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.496+1847C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746565 | ||||||
| chr19:16746576
|
G | A | 2 | a0001c0002t0007g0030a0001c0002t0011g0105 | 2 | HG02015.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.496+1858G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746576 | ||||||
| chr19:16746614
|
A | G | 29 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(26): Show | 29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1896A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746614 | ||||||
| chr19:16746627
|
C | T | 29 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(26): Show | 29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1909C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746627 | ||||||
| chr19:16746675
|
AC | A | 29 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(26): Show | 29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+1958delC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746675 | ||||||
| chr19:16746676
|
C | A | 8 | a0003c0006t0002g0100a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG01981.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+1958C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746676 | ||||||
| chr19:16746690
|
C | CAAA | 10 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(7): Show | 10 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.496+1974_496+1975i others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16746690 | |||||
| chr19:16746692
|
A | AAAC | 19 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(16): Show | 19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+1974_496+1975i others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746692 | ||||||
| chr19:16746692
|
AC | A | 101 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(98): Show | 101 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.496+1975delC | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746692 | ||||||
| chr19:16746693
|
C | A | 39 | a0001c0035t0002g0020a0002c0001t0004g0108a0002c0001t0004g0111others(36): Show | 39 | HG00735.hp1 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.496+1975C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746693 | ||||||
| chr19:16746835
|
A | G | 1 | a0001c0008t0001g0145 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.496+2117A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16746835 | ||||||
| chr19:16747039
|
C | CT | 95 | a0001c0002t0002g0007a0001c0008t0001g0134a0001c0008t0001g0135others(92): Show | 95 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.497-2085dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747039 | |||||
| chr19:16747039
|
CT | C | 14 | a0001c0022t0002g0102a0002c0001t0005g0246a0003c0003t0002g0117others(11): Show | 14 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.497-2085delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747039 | |||||
| chr19:16747186
|
G | A | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-1953G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747186 | ||||||
| chr19:16747243
|
C | G | 1 | a0026c0040t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.497-1896C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747243 | ||||||
| chr19:16747252
|
G | A | 10 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(7): Show | 10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1887G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747252 | ||||||
| chr19:16747279
|
C | A | 6 | a0001c0035t0002g0020a0011c0011t0001g0247a0011c0011t0002g0022others(3): Show | 6 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-1860C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747279 | ||||||
| chr19:16747282
|
G | A | 3 | a0017c0021t0001g0231a0017c0021t0002g0046a0017c0021t0002g0051 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.497-1857G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747282 | ||||||
| chr19:16747333
|
C | T | 10 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(7): Show | 10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1806C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747333 | ||||||
| chr19:16747345
|
T | TTTTA | 32 | a0001c0002t0001g0175a0001c0002t0001g0179a0001c0002t0001g0196others(29): Show | 32 | HG00280.hp1 HG00597.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.497-1757_497-1754d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | |||||
| chr19:16747345
|
T | TTTTATTT others(5): Show |
1 | a0033c0052t0001g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.497-1765_497-1754d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | |||||
| chr19:16747345
|
TTTTA | T | 57 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(54): Show | 57 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.497-1757_497-1754d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | |||||
| chr19:16747345
|
TTTTATTT others(1): Show |
T | 71 | a0001c0035t0002g0020a0003c0006t0002g0086a0004c0005t0001g0296others(68): Show | 71 | HG00642.hp2 HG00733.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.497-1761_497-1754d others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | |||||
| chr19:16747345
|
TTTTATTT others(5): Show |
T | 1 | a0031c0030t0001g0158 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.497-1765_497-1754d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16747345 | |||||
| chr19:16747386
|
A | T | 2 | a0039c0057t0026g0202a0041c0065t0032g0166 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.497-1753A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747386 | ||||||
| chr19:16747447
|
G | A | 10 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(7): Show | 10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1692G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747447 | ||||||
| chr19:16747448
|
C | T | 32 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(29): Show | 32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.497-1691C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747448 | ||||||
| chr19:16747739
|
C | A | 31 | a0001c0002t0001g0201a0004c0009t0005g0140a0004c0009t0005g0224others(28): Show | 31 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.497-1400C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747739 | ||||||
| chr19:16747793
|
T | C | 1 | a0004c0005t0022g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.497-1346T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747793 | ||||||
| chr19:16747872
|
T | C | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-1267T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747872 | ||||||
| chr19:16747910
|
A | G | 1 | a0003c0003t0003g0143 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.497-1229A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16747910 | ||||||
| chr19:16748006
|
T | C | 41 | a0001c0002t0001g0201a0004c0009t0005g0140a0004c0009t0005g0224others(38): Show | 41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-1133T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748006 | ||||||
| chr19:16748127
|
G | A | 10 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(7): Show | 10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-1012G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748127 | ||||||
| chr19:16748141
|
G | A | 11 | a0004c0005t0006g0211a0004c0005t0006g0225a0004c0005t0006g0227others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.497-998G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748141 | ||||||
| chr19:16748173
|
A | G | 41 | a0001c0002t0001g0201a0004c0009t0005g0140a0004c0009t0005g0224others(38): Show | 41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-966A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748173 | ||||||
| chr19:16748176
|
G | A | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.497-963G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748176 | ||||||
| chr19:16748264
|
A | G | 41 | a0001c0002t0001g0201a0004c0009t0005g0140a0004c0009t0005g0224others(38): Show | 41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-875A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748264 | ||||||
| chr19:16748272
|
C | T | 2 | a0010c0013t0008g0194a0010c0013t0009g0045 | 2 | HG00735.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.497-867C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748272 | ||||||
| chr19:16748566
|
C | T | 1 | a0004c0005t0006g0225 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-573C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748566 | ||||||
| chr19:16748716
|
C | T | 2 | a0004c0009t0005g0140a0004c0009t0005g0224 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.497-423C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748716 | ||||||
| chr19:16748823
|
C | CAAT | 11 | a0001c0002t0002g0007a0001c0002t0005g0130a0001c0002t0005g0192others(8): Show | 11 | HG01433.hp1 HG01433.hp2 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.497-301_497-299dup others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16748823 | |||||
| chr19:16748838
|
T | G | 29 | a0001c0002t0001g0142a0001c0002t0001g0170a0001c0002t0001g0189others(26): Show | 29 | HG00099.hp1 HG01071.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.497-301T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748838 | ||||||
| chr19:16748838
|
TAAG | T | 30 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(27): Show | 30 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.497-292_497-290del others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16748838 | |||||
| chr19:16748841
|
G | T | 16 | a0001c0002t0001g0179a0001c0008t0001g0135a0001c0008t0001g0139others(13): Show | 16 | HG01192.hp2 HG02055.hp2 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.497-298G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748841 | ||||||
| chr19:16748844
|
G | T | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.497-295G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748844 | ||||||
| chr19:16748904
|
C | G | 1 | a0036c0048t0018g0129 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.497-235C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748904 | ||||||
| chr19:16748930
|
C | T | 2 | a0004c0009t0013g0206a0006c0014t0002g0015 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.497-209C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16748930 | ||||||
| chr19:16749008
|
A | G | 41 | a0001c0002t0001g0201a0004c0009t0005g0140a0004c0009t0005g0224others(38): Show | 41 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.497-131A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16749008 | ||||||
| chr19:16749046
|
T | C | 2 | a0013c0018t0017g0294a0013c0018t0017g0295 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.497-93T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16749046 | ||||||
| chr19:16749110
|
C | T | 10 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(7): Show | 10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.497-29C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 5/18 | chr19 | 16749110 | ||||||
| chr19:16750564
|
C | G | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1769+153C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750564 | ||||||
| chr19:16750736
|
A | G | 1 | a0003c0003t0002g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1769+325A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750736 | ||||||
| chr19:16750834
|
C | G | 1 | a0001c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1769+423C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750834 | ||||||
| chr19:16750865
|
T | C | 1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1769+454T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750865 | ||||||
| chr19:16750910
|
AG | A | 13 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1769+500delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750910 | ||||||
| chr19:16750952
|
T | C | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1769+541T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16750952 | ||||||
| chr19:16751093
|
G | A | 32 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(29): Show | 32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+682G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751093 | ||||||
| chr19:16751181
|
G | A | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1769+770G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751181 | ||||||
| chr19:16751224
|
CA | C | 74 | a0001c0002t0003g0163a0001c0002t0004g0033a0001c0008t0001g0134others(71): Show | 74 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1769+830delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751224 | |||||
| chr19:16751224
|
CAA | C | 34 | a0002c0007t0002g0008a0002c0007t0002g0057a0004c0005t0001g0296others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.1769+829_1769+830d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751224 | |||||
| chr19:16751241
|
AT | A | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+831delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751241 | ||||||
| chr19:16751246
|
A | G | 20 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(17): Show | 20 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1769+835A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751246 | ||||||
| chr19:16751432
|
AAAGG | A | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1769+1035_1769+103 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751432 | |||||
| chr19:16751481
|
AAAGG | A | 9 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(6): Show | 9 | HG02280.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1769+1087_1769+109 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751481 | |||||
| chr19:16751540
|
C | T | 1 | a0005c0016t0002g0101 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1769+1129C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751540 | ||||||
| chr19:16751658
|
C | T | 55 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(52): Show | 55 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1769+1247C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751658 | ||||||
| chr19:16751779
|
C | T | 3 | a0002c0001t0005g0155a0002c0001t0005g0245a0002c0001t0014g0187 | 3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.1769+1368C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16751779 | ||||||
| chr19:16751817
|
AGAAG | A | 16 | a0001c0002t0001g0142a0001c0002t0001g0189a0009c0028t0002g0115others(13): Show | 16 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1769+1427_1769+143 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751817 | |||||
| chr19:16751860
|
AAAG | A | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1769+1453_1769+145 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751860 | |||||
| chr19:16751982
|
AAAGG | A | 11 | a0002c0001t0001g0263a0002c0001t0002g0021a0002c0001t0002g0029others(8): Show | 11 | HG02630.hp1 HG02647.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1769+1591_1769+159 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16751982 | |||||
| chr19:16752215
|
G | GT | 21 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1769+1806dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16752215 | |||||
| chr19:16752215
|
G | T | 13 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1769+1804G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752215 | ||||||
| chr19:16752217
|
TG | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+1807delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752217 | ||||||
| chr19:16752218
|
G | T | 34 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(31): Show | 34 | HG01070.hp1 HG01071.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1769+1807G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752218 | ||||||
| chr19:16752252
|
C | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+1841C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752252 | ||||||
| chr19:16752259
|
C | T | 13 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1769+1848C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752259 | ||||||
| chr19:16752270
|
A | G | 6 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1769+1859A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752270 | ||||||
| chr19:16752458
|
C | G | 1 | a0004c0009t0008g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1769+2047C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752458 | ||||||
| chr19:16752526
|
T | TGCATGCC others(10): Show |
74 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(71): Show | 74 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1769+2117_1769+211 others(21): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16752526 | |||||
| chr19:16752590
|
A | G | 1 | a0003c0006t0002g0086 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1769+2179A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752590 | ||||||
| chr19:16752714
|
C | A | 1 | a0005c0004t0002g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1769+2303C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752714 | ||||||
| chr19:16752739
|
G | A | 2 | a0001c0008t0001g0168a0039c0057t0026g0202 | 2 | HG01358.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1769+2328G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752739 | ||||||
| chr19:16752783
|
G | C | 1 | a0002c0001t0001g0242 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1769+2372G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752783 | ||||||
| chr19:16752798
|
A | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1769+2387A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752798 | ||||||
| chr19:16752876
|
G | C | 1 | a0003c0006t0002g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1769+2465G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752876 | ||||||
| chr19:16752892
|
G | A | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+2481G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752892 | ||||||
| chr19:16752951
|
T | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1769+2540T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16752951 | ||||||
| chr19:16753120
|
C | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+2709C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753120 | ||||||
| chr19:16753205
|
A | G | 4 | a0012c0017t0001g0212a0012c0017t0002g0018a0012c0017t0002g0019others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1769+2794A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753205 | ||||||
| chr19:16753553
|
C | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1769+3142C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753553 | ||||||
| chr19:16753571
|
C | A | 2 | a0001c0002t0001g0142a0001c0002t0001g0189 | 2 | NA18963.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1769+3160C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753571 | ||||||
| chr19:16753610
|
G | T | 1 | a0001c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1769+3199G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753610 | ||||||
| chr19:16753829
|
T | TCATC | 93 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0199others(90): Show | 93 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.1769+3454_1769+345 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | |||||
| chr19:16753829
|
T | TCATCCAT others(5): Show |
1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1769+3446_1769+345 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | |||||
| chr19:16753829
|
TCATC | T | 15 | a0003c0003t0002g0091a0009c0028t0002g0115a0009c0028t0034g0258others(12): Show | 15 | HG00642.hp2 HG01496.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1769+3454_1769+345 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | |||||
| chr19:16753829
|
TCATCCAT others(13): Show |
T | 1 | a0002c0001t0001g0197 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1769+3438_1769+345 others(24): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16753829 | |||||
| chr19:16753876
|
T | C | 140 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1769+3465T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16753876 | ||||||
| chr19:16754026
|
TATCC | T | 66 | a0001c0002t0001g0170a0001c0002t0005g0287a0002c0001t0002g0021others(63): Show | 66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1769+3641_1769+364 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754026 | |||||
| chr19:16754303
|
G | A | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1769+3892G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754303 | ||||||
| chr19:16754462
|
T | TTCCA | 28 | a0001c0002t0001g0174a0001c0002t0001g0175a0001c0002t0001g0196others(25): Show | 28 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1769+4094_1769+409 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | |||||
| chr19:16754462
|
T | TTCCATCC others(1): Show |
3 | a0001c0002t0004g0009a0002c0001t0003g0162a0044c0058t0035g0167 | 3 | HG01346.hp1 HG02083.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1769+4090_1769+409 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | |||||
| chr19:16754462
|
TTCCA | T | 88 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(85): Show | 88 | HG00099.hp1 HG00558.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.1769+4094_1769+409 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | |||||
| chr19:16754462
|
TTCCATCC others(1): Show |
T | 32 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(29): Show | 32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+4090_1769+409 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | |||||
| chr19:16754462
|
TTCCATCC others(5): Show |
T | 1 | a0005c0004t0001g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1769+4086_1769+409 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754462 | |||||
| chr19:16754506
|
A | G | 32 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(29): Show | 32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1769+4095A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754506 | ||||||
| chr19:16754513
|
C | G | 2 | a0003c0003t0004g0099a0003c0003t0024g0087 | 2 | NA18966.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1769+4102C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754513 | ||||||
| chr19:16754790
|
T | TCATC | 43 | a0001c0002t0001g0291a0004c0005t0001g0296a0004c0005t0006g0211others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.1769+4406_1770-440 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754790 | |||||
| chr19:16754790
|
T | TCATCCAT others(1): Show |
29 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(26): Show | 29 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1769+4402_1770-440 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16754790 | |||||
| chr19:16754800
|
A | G | 6 | a0009c0029t0002g0297a0009c0029t0002g0298a0009c0069t0043g0299others(3): Show | 6 | HG01891.hp2 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1769+4389A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754800 | ||||||
| chr19:16754921
|
A | G | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1770-4304A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16754921 | ||||||
| chr19:16755124
|
T | C | 14 | a0001c0002t0001g0201a0009c0028t0002g0115a0009c0028t0034g0258others(11): Show | 14 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1770-4101T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755124 | ||||||
| chr19:16755228
|
G | T | 11 | a0001c0002t0004g0033a0001c0033t0002g0012a0003c0003t0004g0062others(8): Show | 11 | HG00609.hp1 HG02155.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1770-3997G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755228 | ||||||
| chr19:16755230
|
G | A | 2 | a0017c0021t0001g0231a0017c0021t0002g0046 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1770-3995G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755230 | ||||||
| chr19:16755251
|
C | G | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1770-3974C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755251 | ||||||
| chr19:16755292
|
C | T | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1770-3933C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755292 | ||||||
| chr19:16755293
|
G | A | 3 | a0017c0021t0001g0231a0017c0021t0002g0046a0017c0021t0002g0051 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1770-3932G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755293 | ||||||
| chr19:16755314
|
C | T | 6 | a0002c0007t0001g0239a0002c0007t0002g0008a0002c0007t0002g0057others(3): Show | 6 | NA18747.hp2 NA18960.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1770-3911C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755314 | ||||||
| chr19:16755523
|
G | A | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1770-3702G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755523 | ||||||
| chr19:16755663
|
C | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1770-3562C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755663 | ||||||
| chr19:16755687
|
C | CTTAT | 6 | a0002c0001t0003g0177a0002c0001t0003g0190a0005c0004t0002g0042others(3): Show | 6 | HG00544.hp1 HG02004.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1770-3510_1770-350 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | |||||
| chr19:16755687
|
C | CTTATTTA others(5): Show |
70 | a0001c0002t0001g0146a0001c0002t0001g0153a0001c0002t0001g0154others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.1770-3518_1770-350 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | |||||
| chr19:16755687
|
C | CTTATTTA others(9): Show |
10 | a0001c0002t0001g0148a0001c0002t0002g0031a0001c0002t0002g0063others(7): Show | 10 | HG00544.hp2 HG01934.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1770-3522_1770-350 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | |||||
| chr19:16755687
|
C | CTTATTTA others(13): Show |
1 | a0002c0001t0001g0159 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1770-3526_1770-350 others(24): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | |||||
| chr19:16755687
|
CTTAT | C | 123 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(120): Show | 123 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.1770-3510_1770-350 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | |||||
| chr19:16755687
|
CTTATTTA others(9): Show |
C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1770-3522_1770-350 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755687 | |||||
| chr19:16755726
|
T | TG | 13 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1770-3495dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16755726 | |||||
| chr19:16755971
|
G | C | 28 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(25): Show | 28 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1770-3254G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16755971 | ||||||
| chr19:16756014
|
T | C | 3 | a0013c0018t0017g0294a0013c0018t0017g0295a0013c0018t0022g0124 | 3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1770-3211T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756014 | ||||||
| chr19:16756031
|
A | G | 3 | a0001c0002t0003g0186a0002c0001t0021g0150a0005c0004t0004g0090 | 3 | HG00597.hp2 NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1770-3194A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756031 | ||||||
| chr19:16756145
|
T | A | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-3080T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756145 | ||||||
| chr19:16756251
|
C | A | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1770-2974C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756251 | ||||||
| chr19:16756346
|
T | C | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1770-2879T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756346 | ||||||
| chr19:16756721
|
C | CAGTACCC others(12): Show |
1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1770-2498_1770-249 others(23): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16756721 | |||||
| chr19:16756831
|
C | A | 1 | a0001c0002t0020g0249 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1770-2394C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756831 | ||||||
| chr19:16756853
|
C | T | 21 | a0002c0001t0024g0109a0004c0009t0005g0140a0004c0009t0005g0224others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1770-2372C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756853 | ||||||
| chr19:16756862
|
C | G | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1770-2363C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756862 | ||||||
| chr19:16756992
|
C | A | 2 | a0001c0002t0001g0291a0029c0038t0015g0055 | 2 | NA18993.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1770-2233C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16756992 | ||||||
| chr19:16757162
|
T | C | 134 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(131): Show | 134 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.1770-2063T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757162 | ||||||
| chr19:16757279
|
C | A | 1 | a0005c0004t0002g0059 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1770-1946C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757279 | ||||||
| chr19:16757360
|
G | A | 21 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1770-1865G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757360 | ||||||
| chr19:16757447
|
A | G | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-1778A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757447 | ||||||
| chr19:16757612
|
G | A | 13 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1770-1613G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757612 | ||||||
| chr19:16757632
|
A | G | 14 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(11): Show | 14 | HG02055.hp1 HG02258.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.1770-1593A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757632 | ||||||
| chr19:16757671
|
A | T | 32 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(29): Show | 32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.1770-1554A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757671 | ||||||
| chr19:16757744
|
G | C | 134 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(131): Show | 134 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.1770-1481G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757744 | ||||||
| chr19:16757917
|
T | A | 1 | a0002c0007t0002g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1770-1308T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757917 | ||||||
| chr19:16757918
|
G | C | 1 | a0002c0007t0002g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1770-1307G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757918 | ||||||
| chr19:16757933
|
T | C | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-1292T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16757933 | ||||||
| chr19:16758051
|
C | CA | 95 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(92): Show | 95 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.1770-1161dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16758051 | |||||
| chr19:16758051
|
C | CAA | 8 | a0004c0060t0002g0125a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG02647.hp1 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1770-1162_1770-116 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16758051 | |||||
| chr19:16758051
|
CA | C | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-1161delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16758051 | |||||
| chr19:16758073
|
G | C | 136 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(133): Show | 136 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.1770-1152G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758073 | ||||||
| chr19:16758152
|
T | C | 136 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(133): Show | 136 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.1770-1073T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758152 | ||||||
| chr19:16758344
|
A | G | 13 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1770-881A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758344 | ||||||
| chr19:16758449
|
A | G | 101 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(98): Show | 101 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.1770-776A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758449 | ||||||
| chr19:16758510
|
C | T | 5 | a0009c0029t0002g0297a0009c0029t0002g0298a0019c0024t0001g0251others(2): Show | 5 | HG01891.hp2 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1770-715C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758510 | ||||||
| chr19:16758628
|
A | G | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-597A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758628 | ||||||
| chr19:16758655
|
C | T | 51 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(48): Show | 51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1770-570C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758655 | ||||||
| chr19:16758849
|
A | G | 33 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(30): Show | 33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.1770-376A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758849 | ||||||
| chr19:16758868
|
C | G | 18 | a0001c0002t0001g0142a0001c0002t0001g0175a0001c0002t0001g0179others(15): Show | 18 | HG00673.hp1 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.1770-357C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758868 | ||||||
| chr19:16758948
|
G | T | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-277G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758948 | ||||||
| chr19:16758965
|
C | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1770-260C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16758965 | ||||||
| chr19:16759003
|
C | CA | 39 | a0001c0002t0001g0179a0001c0002t0001g0191a0001c0002t0001g0218others(36): Show | 39 | HG00597.hp2 HG00673.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.1770-194dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
C | CAA | 8 | a0001c0002t0001g0207a0001c0022t0002g0102a0002c0001t0005g0245others(5): Show | 8 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.1770-195_1770-194d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CA | C | 52 | a0001c0002t0001g0146a0001c0002t0001g0153a0001c0002t0001g0154others(49): Show | 52 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1770-194delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAA | C | 13 | a0004c0060t0002g0125a0008c0010t0002g0114a0008c0010t0010g0131others(10): Show | 13 | HG01361.hp1 HG02559.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1770-196_1770-194d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAAA | C | 14 | a0003c0006t0002g0092a0004c0005t0006g0211a0004c0005t0006g0226others(11): Show | 14 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1770-197_1770-194d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAAAA | C | 27 | a0001c0008t0001g0168a0001c0035t0002g0020a0004c0005t0001g0296others(24): Show | 27 | HG00642.hp2 HG01081.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1770-198_1770-194d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAAAAA | C | 46 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(43): Show | 46 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1770-199_1770-194d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAAAAAA others(3): Show |
C | 19 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(16): Show | 19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.1770-203_1770-194d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAAAAAA others(4): Show |
C | 1 | a0006c0014t0008g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1770-204_1770-194d others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAAAAAA others(5): Show |
C | 1 | a0014c0025t0002g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1770-205_1770-194d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759003
|
CAAAAAAA others(6): Show |
C | 1 | a0014c0025t0002g0049 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1770-206_1770-194d others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr19 | 16759003 | |||||
| chr19:16759072
|
C | G | 11 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1770-153C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16759072 | ||||||
| chr19:16759115
|
T | C | 33 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(30): Show | 33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.1770-110T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16759115 | ||||||
| chr19:16759155
|
T | C | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1770-70T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 6/18 | chr19 | 16759155 | ||||||
| chr19:16759758
|
G | T | 4 | a0006c0044t0001g0255a0017c0021t0001g0231a0017c0021t0002g0046others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973+330G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759758 | ||||||
| chr19:16759759
|
C | T | 4 | a0006c0044t0001g0255a0017c0021t0001g0231a0017c0021t0002g0046others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973+331C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759759 | ||||||
| chr19:16759856
|
C | T | 1 | a0044c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1973+428C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759856 | ||||||
| chr19:16759858
|
G | A | 2 | a0021c0026t0002g0083a0021c0026t0015g0078 | 2 | HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1973+430G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759858 | ||||||
| chr19:16759976
|
G | C | 7 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0013g0206others(4): Show | 7 | HG01109.hp2 HG02886.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973+548G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16759976 | ||||||
| chr19:16760037
|
C | G | 6 | a0001c0002t0002g0010a0001c0002t0002g0013a0001c0002t0003g0200others(3): Show | 6 | HG00597.hp1 HG00609.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1973+609C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760037 | ||||||
| chr19:16760110
|
G | A | 6 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(3): Show | 6 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1973+682G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760110 | ||||||
| chr19:16760128
|
C | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1973+700C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760128 | ||||||
| chr19:16760171
|
G | GACTAA | 19 | a0004c0005t0023g0094a0004c0005t0023g0095a0004c0005t0029g0265others(16): Show | 19 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1973+768_1973+772d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760171 | |||||
| chr19:16760171
|
G | GACTAAAC others(3): Show |
16 | a0002c0001t0004g0108a0004c0005t0001g0296a0004c0005t0006g0211others(13): Show | 16 | HG00735.hp1 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1973+763_1973+772d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760171 | |||||
| chr19:16760171
|
GACTAA | G | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1973+768_1973+772d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760171 | |||||
| chr19:16760229
|
C | CATTTT | 43 | a0001c0002t0001g0207a0001c0002t0003g0186a0001c0002t0020g0249others(40): Show | 43 | HG00544.hp1 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1973+844_1973+848d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
C | CATTTTAT others(3): Show |
21 | a0001c0022t0002g0102a0002c0001t0004g0032a0002c0001t0004g0034others(18): Show | 21 | HG00280.hp1 HG01192.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1973+839_1973+848d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
C | CATTTTAT others(8): Show |
39 | a0001c0002t0004g0011a0002c0001t0001g0171a0002c0001t0003g0176others(36): Show | 39 | HG00323.hp1 HG00558.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.1973+834_1973+848d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
C | CATTTTAT others(13): Show |
16 | a0001c0002t0002g0007a0001c0002t0005g0130a0002c0001t0005g0184others(13): Show | 16 | HG01358.hp1 HG01433.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1973+829_1973+848d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
C | CATTTTAT others(18): Show |
4 | a0001c0002t0005g0192a0001c0002t0007g0041a0009c0029t0002g0297others(1): Show | 4 | HG01975.hp1 HG02257.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1973+824_1973+848d others(27): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
CATTTT | C | 72 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0153others(69): Show | 72 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1973+844_1973+848d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
CATTTTAT others(3): Show |
C | 2 | a0017c0021t0001g0231a0017c0021t0002g0046 | 2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1973+839_1973+848d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
CATTTTAT others(8): Show |
C | 68 | a0001c0002t0002g0123a0001c0008t0001g0134a0001c0008t0001g0135others(65): Show | 68 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1973+834_1973+848d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760229
|
CATTTTAT others(13): Show |
C | 1 | a0002c0001t0002g0029 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1973+829_1973+848d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760229 | |||||
| chr19:16760569
|
CATTTT | C | 4 | a0006c0044t0001g0255a0017c0021t0001g0231a0017c0021t0002g0046others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1973+1151_1973+115 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16760569 | |||||
| chr19:16760682
|
C | A | 1 | a0041c0065t0032g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1973+1254C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760682 | ||||||
| chr19:16760694
|
G | T | 1 | a0030c0043t0009g0023 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1973+1266G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760694 | ||||||
| chr19:16760820
|
C | A | 1 | a0001c0002t0001g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1974-1159C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760820 | ||||||
| chr19:16760827
|
T | A | 1 | a0001c0002t0005g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1974-1152T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760827 | ||||||
| chr19:16760894
|
T | C | 51 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(48): Show | 51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1974-1085T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760894 | ||||||
| chr19:16760896
|
T | C | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-1083T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760896 | ||||||
| chr19:16760911
|
G | A | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-1068G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16760911 | ||||||
| chr19:16761135
|
C | T | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-844C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761135 | ||||||
| chr19:16761174
|
A | C | 14 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(11): Show | 14 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1974-805A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761174 | ||||||
| chr19:16761312
|
T | C | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1974-667T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761312 | ||||||
| chr19:16761348
|
T | C | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-631T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761348 | ||||||
| chr19:16761350
|
C | CTCTT | 28 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(25): Show | 28 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1974-614_1974-611d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761350 | |||||
| chr19:16761358
|
T | TTCTTTCT others(24): Show |
2 | a0006c0014t0002g0015a0010c0013t0009g0045 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(33): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761358
|
T | TTCTTTCT others(28): Show |
7 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0013g0206others(4): Show | 7 | HG00735.hp2 HG02886.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1974-611_1974-610i others(37): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761358
|
T | TTCTTTCT others(32): Show |
2 | a0004c0009t0005g0140a0004c0009t0005g0224 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(41): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761358
|
T | TTCTTTCT others(36): Show |
2 | a0004c0009t0009g0047a0006c0014t0008g0253 | 2 | HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(45): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761358
|
T | TTCTTTCT others(40): Show |
3 | a0010c0013t0013g0172a0010c0013t0013g0173a0030c0043t0009g0023 | 3 | HG02145.hp2 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(49): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761358
|
T | TTCTTTCT others(44): Show |
2 | a0016c0019t0016g0003a0016c0019t0016g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1974-611_1974-610i others(53): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761358
|
T | TTCTTTCT others(48): Show |
1 | a0004c0009t0009g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1974-611_1974-610i others(57): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761358
|
T | TTCTTTCT others(52): Show |
1 | a0016c0019t0008g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1974-611_1974-610i others(61): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761358 | |||||
| chr19:16761440
|
C | T | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-539C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761440 | ||||||
| chr19:16761475
|
T | A | 5 | a0002c0001t0004g0032a0002c0001t0004g0034a0002c0001t0004g0035others(2): Show | 5 | HG01975.hp2 HG02273.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1974-504T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761475 | ||||||
| chr19:16761514
|
G | A | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-465G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761514 | ||||||
| chr19:16761534
|
C | CT | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-437dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761534 | |||||
| chr19:16761610
|
G | A | 55 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(52): Show | 55 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1974-369G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761610 | ||||||
| chr19:16761685
|
C | T | 3 | a0003c0006t0002g0092a0014c0025t0002g0048a0014c0025t0002g0049 | 3 | HG02280.hp2 HG04115.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1974-294C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761685 | ||||||
| chr19:16761701
|
G | A | 51 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(48): Show | 51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1974-278G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761701 | ||||||
| chr19:16761804
|
GA | G | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1974-165delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16761804 | |||||
| chr19:16761947
|
C | G | 1 | a0002c0001t0005g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1974-32C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 7/18 | chr19 | 16761947 | ||||||
| chr19:16762195
|
C | G | 1 | a0001c0002t0001g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2133+57C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762195 | ||||||
| chr19:16762287
|
C | T | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2133+149C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762287 | ||||||
| chr19:16762292
|
C | A | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2133+154C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762292 | ||||||
| chr19:16762297
|
C | CT | 9 | a0001c0002t0003g0267a0002c0001t0001g0137a0004c0005t0006g0228others(6): Show | 9 | HG01175.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.2133+176dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | |||||
| chr19:16762297
|
C | CTT | 35 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(32): Show | 35 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(32): Show |
intron_variant | MODIFIER | c.2133+175_2133+176d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | |||||
| chr19:16762297
|
C | CTTT | 6 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(3): Show | 6 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.2133+174_2133+176d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | |||||
| chr19:16762297
|
C | CTTTT | 7 | a0001c0008t0001g0139a0001c0008t0027g0136a0001c0022t0001g0151others(4): Show | 7 | HG01496.hp1 HG02886.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.2133+173_2133+176d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | |||||
| chr19:16762297
|
C | CTTTTT | 48 | a0001c0008t0001g0135a0001c0008t0001g0145a0001c0008t0001g0168others(45): Show | 48 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.2133+172_2133+176d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | |||||
| chr19:16762297
|
CT | C | 11 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0013g0206others(8): Show | 11 | HG01109.hp2 HG02040.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2133+176delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762297 | |||||
| chr19:16762298
|
T | TTTTC | 9 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2133+163_2133+164i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762298 | |||||
| chr19:16762335
|
C | T | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2133+197C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762335 | ||||||
| chr19:16762336
|
G | A | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2133+198G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762336 | ||||||
| chr19:16762357
|
C | T | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2133+219C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762357 | ||||||
| chr19:16762361
|
A | G | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2133+223A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762361 | ||||||
| chr19:16762442
|
A | G | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2133+304A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762442 | ||||||
| chr19:16762555
|
A | AAAAC | 33 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(30): Show | 33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.2133+433_2133+436d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16762555 | |||||
| chr19:16762594
|
T | C | 1 | a0002c0001t0001g0160 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2133+456T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762594 | ||||||
| chr19:16762774
|
C | T | 1 | a0004c0009t0008g0286 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2133+636C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762774 | ||||||
| chr19:16762798
|
C | T | 3 | a0002c0001t0005g0155a0002c0001t0005g0245a0002c0001t0014g0187 | 3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2133+660C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762798 | ||||||
| chr19:16762917
|
G | C | 1 | a0001c0002t0011g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2133+779G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762917 | ||||||
| chr19:16762925
|
A | G | 33 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(30): Show | 33 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.2133+787A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16762925 | ||||||
| chr19:16763165
|
G | A | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2134-663G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763165 | ||||||
| chr19:16763183
|
C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2134-645C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763183 | ||||||
| chr19:16763231
|
C | G | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2134-597C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763231 | ||||||
| chr19:16763320
|
C | T | 51 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(48): Show | 51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2134-508C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763320 | ||||||
| chr19:16763491
|
A | G | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2134-337A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763491 | ||||||
| chr19:16763694
|
G | A | 11 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0199others(8): Show | 11 | HG00544.hp2 HG02027.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.2134-134G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763694 | ||||||
| chr19:16763697
|
G | T | 1 | a0002c0001t0005g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2134-131G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763697 | ||||||
| chr19:16763699
|
A | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2134-129A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763699 | ||||||
| chr19:16763713
|
T | C | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2134-115T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 8/18 | chr19 | 16763713 | ||||||
| chr19:16763977
|
G | A | 1 | a0003c0003t0002g0091 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2251+32G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16763977 | ||||||
| chr19:16763994
|
C | T | 2 | a0007c0012t0001g0234a0007c0012t0001g0235 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2251+49C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16763994 | ||||||
| chr19:16763995
|
G | A | 1 | a0002c0007t0002g0122 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2251+50G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16763995 | ||||||
| chr19:16764047
|
C | G | 2 | a0016c0019t0016g0003a0016c0019t0016g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2251+102C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764047 | ||||||
| chr19:16764199
|
A | G | 1 | a0010c0013t0008g0194 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2251+254A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764199 | ||||||
| chr19:16764265
|
C | A | 1 | a0002c0001t0003g0237 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2251+320C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764265 | ||||||
| chr19:16764278
|
A | C | 1 | a0001c0002t0001g0157 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2251+333A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764278 | ||||||
| chr19:16764304
|
C | T | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2251+359C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764304 | ||||||
| chr19:16764324
|
C | T | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2251+379C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764324 | ||||||
| chr19:16764349
|
C | T | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2251+404C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764349 | ||||||
| chr19:16764360
|
T | TGTCC | 17 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(14): Show | 17 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.2251+416_2251+419d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764360 | |||||
| chr19:16764361
|
G | GTCCA | 58 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2251+455_2251+458d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | |||||
| chr19:16764361
|
G | GTCCATCC others(1): Show |
4 | a0001c0002t0001g0193a0001c0002t0012g0198a0003c0003t0002g0076others(1): Show | 4 | HG00558.hp2 NA18945.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2251+451_2251+458d others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | |||||
| chr19:16764361
|
GTCCA | G | 71 | a0001c0008t0001g0145a0001c0008t0001g0168a0001c0008t0001g0270others(68): Show | 71 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.2251+455_2251+458d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | |||||
| chr19:16764361
|
GTCCATCC others(1): Show |
G | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+451_2251+458d others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | |||||
| chr19:16764361
|
GTCCATCC others(5): Show |
G | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2251+447_2251+458d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | |||||
| chr19:16764361
|
GTCCATCC others(13): Show |
G | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2251+439_2251+458d others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764361 | |||||
| chr19:16764365
|
A | G | 11 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(8): Show | 11 | HG02132.hp2 HG02965.hp2 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.2251+420A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764365 | ||||||
| chr19:16764369
|
A | G | 67 | a0001c0008t0001g0145a0001c0008t0001g0168a0001c0008t0001g0270others(64): Show | 67 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.2251+424A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764369 | ||||||
| chr19:16764373
|
A | G | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2251+428A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764373 | ||||||
| chr19:16764377
|
A | G | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2251+432A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764377 | ||||||
| chr19:16764385
|
A | G | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2251+440A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764385 | ||||||
| chr19:16764392
|
CATCCATC others(5): Show |
C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2251+449_2251+460d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764392 | |||||
| chr19:16764415
|
T | C | 18 | a0002c0001t0004g0032a0002c0001t0004g0034a0002c0001t0004g0035others(15): Show | 18 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.2251+470T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764415 | ||||||
| chr19:16764466
|
A | ACCAT | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2252-544_2252-541d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr19 | 16764466 | |||||
| chr19:16764777
|
C | T | 72 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(69): Show | 72 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.2252-257C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 9/18 | chr19 | 16764777 | ||||||
| chr19:16765288
|
T | C | 255 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.2410+96T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765288 | ||||||
| chr19:16765293
|
A | G | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2410+101A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765293 | ||||||
| chr19:16765305
|
T | C | 1 | a0008c0010t0010g0278 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2410+113T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765305 | ||||||
| chr19:16765401
|
G | A | 2 | a0004c0005t0006g0228a0004c0005t0006g0230 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2410+209G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765401 | ||||||
| chr19:16765415
|
C | T | 1 | a0001c0002t0001g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2410+223C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765415 | ||||||
| chr19:16765550
|
T | C | 51 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(48): Show | 51 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2410+358T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765550 | ||||||
| chr19:16765592
|
C | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2410+400C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765592 | ||||||
| chr19:16765690
|
G | A | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2410+498G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765690 | ||||||
| chr19:16765704
|
G | A | 69 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(66): Show | 69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+512G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765704 | ||||||
| chr19:16765745
|
G | A | 1 | a0008c0010t0010g0278 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2410+553G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765745 | ||||||
| chr19:16765966
|
G | A | 4 | a0006c0044t0001g0255a0017c0021t0001g0231a0017c0021t0002g0046others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2410+774G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765966 | ||||||
| chr19:16765972
|
G | A | 1 | a0022c0042t0001g0152 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2410+780G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16765972 | ||||||
| chr19:16766016
|
C | CA | 18 | a0001c0002t0001g0174a0001c0002t0001g0193a0001c0002t0002g0010others(15): Show | 18 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.2410+843dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766016 | |||||
| chr19:16766016
|
CA | C | 76 | a0001c0002t0004g0033a0001c0008t0001g0134a0001c0008t0001g0135others(73): Show | 76 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.2410+843delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766016 | |||||
| chr19:16766032
|
A | G | 69 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(66): Show | 69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+840A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766032 | ||||||
| chr19:16766036
|
G | A | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2410+844G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766036 | ||||||
| chr19:16766161
|
TATA | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2410+977_2410+979d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766161 | |||||
| chr19:16766172
|
C | T | 1 | a0021c0026t0015g0078 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2410+980C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766172 | ||||||
| chr19:16766277
|
C | T | 2 | a0002c0001t0001g0159a0002c0001t0020g0289 | 2 | HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2410+1085C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766277 | ||||||
| chr19:16766522
|
T | C | 69 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(66): Show | 69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+1330T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766522 | ||||||
| chr19:16766553
|
GGTTTT | G | 69 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(66): Show | 69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+1367_2410+137 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766553 | |||||
| chr19:16766554
|
G | A | 1 | a0001c0002t0004g0033 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2410+1362G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16766554 | ||||||
| chr19:16766591
|
AT | A | 159 | a0001c0002t0003g0144a0001c0002t0003g0163a0001c0002t0003g0200others(156): Show | 159 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.2410+1411delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16766591 | |||||
| chr19:16767014
|
C | G | 1 | a0001c0002t0001g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2410+1822C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767014 | ||||||
| chr19:16767024
|
A | G | 1 | a0032c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2410+1832A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767024 | ||||||
| chr19:16767100
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2410+1908C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767100 | ||||||
| chr19:16767164
|
C | T | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2410+1972C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767164 | ||||||
| chr19:16767167
|
C | CT | 18 | a0001c0002t0003g0267a0001c0002t0004g0011a0002c0001t0001g0171others(15): Show | 18 | HG00597.hp2 HG01081.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.2410+2002dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | |||||
| chr19:16767167
|
CT | C | 100 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.2410+2002delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | |||||
| chr19:16767167
|
CTT | C | 50 | a0001c0002t0002g0007a0001c0008t0001g0134a0001c0008t0001g0135others(47): Show | 50 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.2410+2001_2410+200 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | |||||
| chr19:16767167
|
CTTT | C | 12 | a0008c0010t0010g0131a0008c0010t0010g0278a0008c0010t0010g0284others(9): Show | 12 | HG02109.hp1 HG02293.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2410+2000_2410+200 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | |||||
| chr19:16767167
|
CTTTTTT | C | 50 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(47): Show | 50 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2410+1997_2410+200 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | |||||
| chr19:16767167
|
CTTTTTTT others(5): Show |
C | 9 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2410+1991_2410+200 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | |||||
| chr19:16767167
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0022t0001g0151a0001c0022t0002g0102a0022c0042t0001g0152others(1): Show | 4 | HG01496.hp1 NA18993.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2410+1990_2410+200 others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767167 | |||||
| chr19:16767219
|
G | A | 8 | a0004c0005t0048g0002a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG02055.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2410+2027G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767219 | ||||||
| chr19:16767294
|
C | A | 5 | a0001c0002t0004g0009a0001c0002t0004g0033a0001c0033t0002g0012others(2): Show | 5 | HG00597.hp1 HG00609.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.2410+2102C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767294 | ||||||
| chr19:16767364
|
C | T | 2 | a0005c0004t0003g0248a0005c0004t0004g0097 | 2 | HG00280.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2410+2172C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767364 | ||||||
| chr19:16767476
|
G | A | 1 | a0005c0004t0002g0042 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2410+2284G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767476 | ||||||
| chr19:16767543
|
C | T | 69 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(66): Show | 69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+2351C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767543 | ||||||
| chr19:16767561
|
C | G | 138 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(135): Show | 138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+2369C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767561 | ||||||
| chr19:16767593
|
G | A | 9 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2410+2401G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767593 | ||||||
| chr19:16767650
|
C | T | 69 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(66): Show | 69 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.2410+2458C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767650 | ||||||
| chr19:16767713
|
C | T | 1 | a0001c0002t0001g0175 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2410+2521C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767713 | ||||||
| chr19:16767771
|
A | T | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2410+2579A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767771 | ||||||
| chr19:16767797
|
C | A | 2 | a0001c0002t0001g0196a0001c0002t0001g0218 | 2 | HG02056.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2410+2605C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767797 | ||||||
| chr19:16767816
|
T | A | 1 | a0001c0002t0001g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2410+2624T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767816 | ||||||
| chr19:16767894
|
G | A | 15 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(12): Show | 15 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2410+2702G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16767894 | ||||||
| chr19:16767982
|
C | CT | 53 | a0001c0002t0001g0142a0001c0002t0001g0153a0001c0002t0001g0175others(50): Show | 53 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.2410+2815dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | |||||
| chr19:16767982
|
CT | C | 77 | a0001c0002t0012g0203a0001c0008t0001g0135a0001c0008t0001g0139others(74): Show | 77 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2410+2815delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | |||||
| chr19:16767982
|
CTT | C | 6 | a0001c0002t0002g0007a0002c0007t0001g0239a0007c0012t0001g0232others(3): Show | 6 | HG02818.hp1 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2410+2814_2410+281 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | |||||
| chr19:16767982
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0001t0001g0137 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2410+2803_2410+281 others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16767982 | |||||
| chr19:16768068
|
C | T | 140 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(137): Show | 140 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.2410+2876C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768068 | ||||||
| chr19:16768135
|
C | T | 13 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2410+2943C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768135 | ||||||
| chr19:16768149
|
C | A | 2 | a0005c0004t0003g0248a0005c0004t0004g0097 | 2 | HG00280.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.2410+2957C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768149 | ||||||
| chr19:16768216
|
G | A | 1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2410+3024G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768216 | ||||||
| chr19:16768232
|
G | A | 1 | a0047c0055t0037g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2410+3040G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768232 | ||||||
| chr19:16768291
|
TGGCTAAG others(18): Show |
T | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2410+3122_2410+314 others(29): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16768291 | |||||
| chr19:16768333
|
C | T | 1 | a0003c0003t0044g0070 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2410+3141C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768333 | ||||||
| chr19:16768389
|
G | A | 13 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2410+3197G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768389 | ||||||
| chr19:16768406
|
C | T | 1 | a0008c0010t0010g0278 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2410+3214C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768406 | ||||||
| chr19:16768450
|
T | C | 1 | a0002c0001t0005g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2410+3258T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768450 | ||||||
| chr19:16768453
|
A | C | 1 | a0002c0001t0001g0263 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2410+3261A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768453 | ||||||
| chr19:16768462
|
A | C | 138 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(135): Show | 138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+3270A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768462 | ||||||
| chr19:16768569
|
C | G | 1 | a0016c0019t0008g0257 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2410+3377C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768569 | ||||||
| chr19:16768601
|
T | TAAACTAA others(3): Show |
299 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.2410+3411_2410+341 others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16768601 | |||||
| chr19:16768700
|
G | A | 1 | a0009c0028t0002g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2410+3508G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768700 | ||||||
| chr19:16768720
|
A | C | 1 | a0002c0001t0005g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2410+3528A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768720 | ||||||
| chr19:16768740
|
C | G | 138 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(135): Show | 138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+3548C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768740 | ||||||
| chr19:16768795
|
G | A | 10 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(7): Show | 10 | HG02647.hp1 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2410+3603G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768795 | ||||||
| chr19:16768858
|
C | T | 13 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2410+3666C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768858 | ||||||
| chr19:16768895
|
A | G | 138 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(135): Show | 138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2410+3703A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768895 | ||||||
| chr19:16768991
|
T | C | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2410+3799T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16768991 | ||||||
| chr19:16769332
|
C | T | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2411-3794C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769332 | ||||||
| chr19:16769459
|
T | TA | 49 | a0001c0022t0001g0151a0001c0022t0002g0102a0002c0007t0002g0008others(46): Show | 49 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(46): Show |
intron_variant | MODIFIER | c.2411-3655dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16769459 | |||||
| chr19:16769459
|
T | TAA | 69 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(66): Show | 69 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2411-3656_2411-365 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16769459 | |||||
| chr19:16769459
|
TA | T | 71 | a0001c0002t0001g0148a0001c0002t0001g0153a0001c0002t0001g0154others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2411-3655delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16769459 | |||||
| chr19:16769515
|
G | T | 1 | a0001c0022t0001g0151 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2411-3611G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769515 | ||||||
| chr19:16769653
|
G | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2411-3473G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769653 | ||||||
| chr19:16769673
|
C | T | 56 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(53): Show | 56 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.2411-3453C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769673 | ||||||
| chr19:16769698
|
ACTTTGGA others(47): Show |
A | 1 | a0003c0003t0024g0087 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2411-3427_2411-337 others(58): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769698 | ||||||
| chr19:16769734
|
G | A | 4 | a0012c0017t0001g0212a0012c0017t0002g0018a0012c0017t0002g0019others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2411-3392G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769734 | ||||||
| chr19:16769770
|
T | C | 1 | a0002c0007t0002g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2411-3356T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769770 | ||||||
| chr19:16769969
|
C | G | 4 | a0012c0017t0001g0212a0012c0017t0002g0018a0012c0017t0002g0019others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2411-3157C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16769969 | ||||||
| chr19:16770027
|
C | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-3099C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770027 | ||||||
| chr19:16770090
|
G | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-3036G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770090 | ||||||
| chr19:16770144
|
T | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2411-2982T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770144 | ||||||
| chr19:16770162
|
G | A | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-2964G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770162 | ||||||
| chr19:16770354
|
C | T | 8 | a0001c0002t0004g0011a0002c0001t0003g0176a0002c0001t0003g0183others(5): Show | 8 | HG01081.hp2 HG01257.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2411-2772C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770354 | ||||||
| chr19:16770498
|
G | A | 49 | a0001c0002t0003g0144a0001c0008t0001g0134a0001c0008t0001g0135others(46): Show | 49 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.2411-2628G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770498 | ||||||
| chr19:16770553
|
C | G | 138 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(135): Show | 138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2411-2573C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770553 | ||||||
| chr19:16770568
|
G | A | 1 | a0026c0040t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2411-2558G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770568 | ||||||
| chr19:16770839
|
T | C | 1 | a0001c0031t0001g0156 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2411-2287T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16770839 | ||||||
| chr19:16771021
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-2105C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771021 | ||||||
| chr19:16771054
|
C | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2411-2072C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771054 | ||||||
| chr19:16771083
|
A | G | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2411-2043A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771083 | ||||||
| chr19:16771189
|
C | T | 1 | a0011c0011t0011g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2411-1937C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771189 | ||||||
| chr19:16771232
|
G | T | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2411-1894G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771232 | ||||||
| chr19:16771321
|
A | G | 54 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(51): Show | 54 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.2411-1805A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771321 | ||||||
| chr19:16771359
|
A | C | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2411-1767A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771359 | ||||||
| chr19:16771610
|
T | G | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-1516T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771610 | ||||||
| chr19:16771618
|
A | G | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2411-1508A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771618 | ||||||
| chr19:16771746
|
C | T | 19 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(16): Show | 19 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.2411-1380C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771746 | ||||||
| chr19:16771831
|
C | CT | 62 | a0001c0002t0001g0146a0001c0002t0001g0170a0001c0002t0001g0208others(59): Show | 62 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.2411-1277dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771831 | |||||
| chr19:16771831
|
C | CTT | 6 | a0004c0005t0023g0094a0004c0005t0023g0095a0004c0005t0029g0265others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2411-1278_2411-127 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771831 | |||||
| chr19:16771831
|
CT | C | 9 | a0001c0002t0005g0192a0002c0001t0001g0261a0004c0009t0005g0140others(6): Show | 9 | HG01167.hp1 HG01167.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.2411-1277delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771831 | |||||
| chr19:16771858
|
G | GCCTCGCT others(5): Show |
1 | a0001c0002t0011g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2411-1267_2411-125 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16771858 | |||||
| chr19:16771949
|
C | A | 3 | a0013c0018t0017g0294a0013c0018t0017g0295a0013c0018t0022g0124 | 3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2411-1177C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771949 | ||||||
| chr19:16771959
|
G | A | 1 | a0001c0002t0001g0193 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2411-1167G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16771959 | ||||||
| chr19:16772054
|
C | T | 1 | a0010c0039t0001g0161 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2411-1072C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772054 | ||||||
| chr19:16772140
|
A | T | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-986A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772140 | ||||||
| chr19:16772377
|
T | C | 1 | a0044c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2411-749T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772377 | ||||||
| chr19:16772507
|
C | G | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-619C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772507 | ||||||
| chr19:16772575
|
G | C | 1 | a0042c0066t0008g0264 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2411-551G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772575 | ||||||
| chr19:16772585
|
G | T | 1 | a0032c0053t0001g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2411-541G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772585 | ||||||
| chr19:16772686
|
T | C | 1 | a0002c0007t0049g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2411-440T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16772686 | ||||||
| chr19:16773101
|
C | T | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2411-25C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 10/18 | chr19 | 16773101 | ||||||
| chr19:16773455
|
C | T | 1 | a0002c0001t0003g0162 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2608+132C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16773455 | ||||||
| chr19:16773809
|
CA | C | 13 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+487delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16773809 | ||||||
| chr19:16773923
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+600C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16773923 | ||||||
| chr19:16773939
|
T | TATCC | 28 | a0001c0002t0001g0142a0001c0002t0001g0189a0001c0002t0001g0201others(25): Show | 28 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.2608+651_2608+654d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773939 | |||||
| chr19:16773939
|
TATCC | T | 67 | a0001c0002t0007g0030a0001c0008t0001g0134a0001c0008t0001g0135others(64): Show | 67 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.2608+651_2608+654d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773939 | |||||
| chr19:16773939
|
TATCCATC others(9): Show |
T | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+639_2608+654d others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773939 | |||||
| chr19:16773976
|
A | ATTAATTC others(8): Show |
1 | a0003c0003t0004g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2608+654_2608+668d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16773976 | |||||
| chr19:16774050
|
C | G | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2608+727C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774050 | ||||||
| chr19:16774082
|
C | T | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2608+759C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774082 | ||||||
| chr19:16774083
|
T | C | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2608+760T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774083 | ||||||
| chr19:16774284
|
C | T | 1 | a0018c0023t0005g0240 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2608+961C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774284 | ||||||
| chr19:16774299
|
T | C | 1 | a0002c0001t0020g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2608+976T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774299 | ||||||
| chr19:16774306
|
A | G | 12 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(9): Show | 12 | HG02280.hp2 HG02647.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.2608+983A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774306 | ||||||
| chr19:16774326
|
C | CTCCA | 68 | a0003c0003t0002g0065a0004c0005t0001g0296a0004c0005t0006g0211others(65): Show | 68 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.2608+1023_2608+102 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16774326 | |||||
| chr19:16774358
|
A | T | 1 | a0004c0005t0006g0227 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2608+1035A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774358 | ||||||
| chr19:16774466
|
TCCATCCA others(1): Show |
T | 18 | a0001c0002t0003g0186a0001c0002t0004g0011a0001c0002t0012g0198others(15): Show | 18 | HG00597.hp2 HG01081.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.2608+1159_2608+116 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16774466 | |||||
| chr19:16774509
|
T | C | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+1186T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774509 | ||||||
| chr19:16774511
|
C | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608+1188C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774511 | ||||||
| chr19:16774554
|
C | T | 1 | a0042c0066t0008g0264 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2608+1231C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774554 | ||||||
| chr19:16774659
|
C | T | 2 | a0001c0002t0005g0192a0001c0002t0007g0041 | 2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2608+1336C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774659 | ||||||
| chr19:16774730
|
A | G | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608+1407A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774730 | ||||||
| chr19:16774735
|
T | C | 3 | a0013c0018t0017g0294a0013c0018t0017g0295a0013c0018t0022g0124 | 3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2608+1412T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774735 | ||||||
| chr19:16774760
|
C | T | 1 | a0003c0003t0003g0288 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2608+1437C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774760 | ||||||
| chr19:16774769
|
C | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+1446C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16774769 | ||||||
| chr19:16775035
|
C | A | 1 | a0007c0067t0003g0277 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2608+1712C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775035 | ||||||
| chr19:16775180
|
A | T | 1 | a0003c0003t0004g0026 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2608+1857A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775180 | ||||||
| chr19:16775210
|
G | A | 13 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+1887G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775210 | ||||||
| chr19:16775264
|
G | T | 3 | a0003c0006t0002g0072a0005c0016t0002g0056a0027c0032t0001g0269 | 3 | HG00642.hp1 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2608+1941G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775264 | ||||||
| chr19:16775300
|
T | TA | 22 | a0003c0003t0044g0070a0004c0009t0009g0047a0008c0010t0002g0114others(19): Show | 22 | HG01192.hp2 HG02040.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2608+1986dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16775300 | |||||
| chr19:16775300
|
T | TAA | 47 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(44): Show | 47 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.2608+1985_2608+198 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16775300 | |||||
| chr19:16775389
|
G | A | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2066G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775389 | ||||||
| chr19:16775434
|
C | CT | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2111_2608+211 others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775434 | ||||||
| chr19:16775442
|
C | T | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2608+2119C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775442 | ||||||
| chr19:16775455
|
G | GGGCTGTC others(15): Show |
1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2608+2133_2608+215 others(26): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16775455 | |||||
| chr19:16775466
|
G | A | 17 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(14): Show | 17 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.2608+2143G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775466 | ||||||
| chr19:16775700
|
T | C | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2377T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775700 | ||||||
| chr19:16775730
|
G | A | 21 | a0003c0003t0044g0070a0004c0009t0005g0140a0004c0009t0005g0224others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2608+2407G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775730 | ||||||
| chr19:16775865
|
A | G | 4 | a0001c0002t0001g0142a0001c0002t0001g0189a0001c0002t0001g0201others(1): Show | 4 | NA18963.hp1 NA18963.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.2608+2542A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16775865 | ||||||
| chr19:16776203
|
G | A | 71 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(68): Show | 71 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2608+2880G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776203 | ||||||
| chr19:16776276
|
T | A | 138 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(135): Show | 138 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.2608+2953T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776276 | ||||||
| chr19:16776322
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2608+2999C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776322 | ||||||
| chr19:16776330
|
G | A | 13 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(10): Show | 13 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.2608+3007G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776330 | ||||||
| chr19:16776424
|
C | CG | 3 | a0001c0022t0002g0102a0002c0007t0002g0008a0017c0021t0002g0046 | 3 | HG03516.hp1 NA18993.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2609-2916dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776424 | |||||
| chr19:16776424
|
C | T | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2609-2919C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776424 | ||||||
| chr19:16776484
|
C | T | 3 | a0001c0002t0001g0142a0001c0002t0001g0201a0025c0034t0001g0133 | 3 | NA18963.hp2 NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2609-2859C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776484 | ||||||
| chr19:16776546
|
C | T | 1 | a0002c0001t0003g0236 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2609-2797C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776546 | ||||||
| chr19:16776569
|
C | CA | 48 | a0001c0002t0012g0203a0001c0022t0002g0102a0002c0001t0001g0137others(45): Show | 48 | HG00642.hp2 HG01081.hp1 HG01257.hp2 others(45): Show |
intron_variant | MODIFIER | c.2609-2760dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776569 | |||||
| chr19:16776569
|
CA | C | 6 | a0001c0002t0007g0030a0002c0001t0003g0183a0006c0014t0002g0015others(3): Show | 6 | HG01109.hp2 HG02040.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2609-2760delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776569 | |||||
| chr19:16776584
|
T | A | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2759T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776584 | ||||||
| chr19:16776611
|
G | T | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2609-2732G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776611 | ||||||
| chr19:16776612
|
T | C | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2609-2731T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776612 | ||||||
| chr19:16776634
|
A | G | 95 | a0001c0002t0001g0142a0001c0002t0001g0148a0001c0002t0001g0153others(92): Show | 95 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.2609-2709A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776634 | ||||||
| chr19:16776718
|
G | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2609-2625G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776718 | ||||||
| chr19:16776773
|
T | TA | 44 | a0001c0022t0001g0151a0001c0022t0002g0102a0001c0035t0002g0020others(41): Show | 44 | HG00642.hp1 HG00642.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.2609-2548dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776773 | |||||
| chr19:16776773
|
TA | T | 51 | a0001c0002t0001g0157a0001c0002t0001g0170a0001c0002t0002g0031others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.2609-2548delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776773 | |||||
| chr19:16776875
|
G | A | 36 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(33): Show | 36 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(33): Show |
intron_variant | MODIFIER | c.2609-2468G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16776875 | ||||||
| chr19:16776941
|
GA | G | 72 | a0001c0008t0002g0044a0004c0005t0001g0296a0004c0005t0006g0211others(69): Show | 72 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.2609-2391delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776941 | |||||
| chr19:16776984
|
AG | A | 3 | a0001c0002t0012g0203a0020c0027t0007g0080a0024c0036t0001g0209 | 3 | HG02083.hp1 NA18946.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2609-2355delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776984 | |||||
| chr19:16776985
|
G | GGGGAAGG others(57): Show |
1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2325_2609-232 others(68): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16776985 | |||||
| chr19:16777108
|
A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2235A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777108 | ||||||
| chr19:16777137
|
G | A | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2206G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777137 | ||||||
| chr19:16777140
|
A | G | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2203A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777140 | ||||||
| chr19:16777141
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2202G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777141 | ||||||
| chr19:16777150
|
AGGGAAGG others(12): Show |
A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2190_2609-217 others(23): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777150 | |||||
| chr19:16777152
|
G | A | 1 | a0002c0001t0001g0180 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2609-2191G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777152 | ||||||
| chr19:16777159
|
G | A | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2184G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777159 | ||||||
| chr19:16777161
|
AGGGAAAG others(20): Show |
A | 4 | a0003c0003t0004g0079a0017c0021t0001g0231a0017c0021t0002g0046others(1): Show | 4 | HG01884.hp2 HG02015.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.2609-2145_2609-211 others(31): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777161 | |||||
| chr19:16777162
|
G | A | 1 | a0002c0001t0001g0260 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2609-2181G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777162 | ||||||
| chr19:16777162
|
G | GGGGAGGA others(5): Show |
1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2179_2609-217 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777162 | |||||
| chr19:16777165
|
A | G | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2178A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777165 | ||||||
| chr19:16777181
|
A | C | 1 | a0001c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-2162A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777181 | ||||||
| chr19:16777188
|
G | A | 2 | a0002c0007t0002g0008a0011c0011t0011g0025 | 2 | HG02559.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2609-2155G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777188 | ||||||
| chr19:16777194
|
A | G | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2149A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777194 | ||||||
| chr19:16777205
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2138G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777205 | ||||||
| chr19:16777215
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2128G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777215 | ||||||
| chr19:16777215
|
G | GGGGAAAG others(35): Show |
1 | a0001c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2609-2118_2609-207 others(46): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777215 | |||||
| chr19:16777219
|
A | G | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2609-2124A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777219 | ||||||
| chr19:16777220
|
AAGGGAAG others(8): Show |
A | 68 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(65): Show | 68 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.2609-2108_2609-209 others(19): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777220 | |||||
| chr19:16777221
|
AGGGAAGG others(7): Show |
A | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2609-2121_2609-210 others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777221 | ||||||
| chr19:16777225
|
A | G | 1 | a0002c0001t0005g0245 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2609-2118A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777225 | ||||||
| chr19:16777230
|
G | A | 2 | a0002c0001t0005g0245a0002c0007t0002g0008 | 2 | HG00558.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2609-2113G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777230 | ||||||
| chr19:16777232
|
G | A | 1 | a0010c0013t0009g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2609-2111G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777232 | ||||||
| chr19:16777235
|
G | A | 2 | a0002c0001t0005g0245a0011c0011t0011g0025 | 2 | HG00558.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2609-2108G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777235 | ||||||
| chr19:16777240
|
A | G | 1 | a0002c0001t0005g0245 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2609-2103A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777240 | ||||||
| chr19:16777250
|
A | G | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2093A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777250 | ||||||
| chr19:16777262
|
A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2081A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777262 | ||||||
| chr19:16777264
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2079G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777264 | ||||||
| chr19:16777267
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2076G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777267 | ||||||
| chr19:16777272
|
A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2071A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777272 | ||||||
| chr19:16777274
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2069G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777274 | ||||||
| chr19:16777274
|
G | T | 4 | a0006c0044t0001g0255a0017c0021t0001g0231a0017c0021t0002g0046others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-2069G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777274 | ||||||
| chr19:16777279
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2064G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777279 | ||||||
| chr19:16777283
|
A | G | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2609-2060A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777283 | ||||||
| chr19:16777284
|
G | A | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2059G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777284 | ||||||
| chr19:16777287
|
A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2056A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777287 | ||||||
| chr19:16777291
|
G | A | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2609-2052G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777291 | ||||||
| chr19:16777294
|
G | A | 1 | a0002c0007t0002g0008 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2609-2049G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777294 | ||||||
| chr19:16777296
|
G | A | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2609-2047G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777296 | ||||||
| chr19:16777318
|
A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2025A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777318 | ||||||
| chr19:16777319
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2024G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777319 | ||||||
| chr19:16777325
|
A | T | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-2018A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777325 | ||||||
| chr19:16777345
|
A | G | 1 | a0015c0020t0005g0222 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2609-1998A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777345 | ||||||
| chr19:16777361
|
AAGGGG | A | 16 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(13): Show | 16 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2609-1970_2609-196 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777361 | |||||
| chr19:16777379
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1964G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777379 | ||||||
| chr19:16777404
|
G | T | 1 | a0024c0036t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2609-1939G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777404 | ||||||
| chr19:16777425
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1918G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777425 | ||||||
| chr19:16777450
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1893G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777450 | ||||||
| chr19:16777453
|
A | G | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2609-1890A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777453 | ||||||
| chr19:16777455
|
T | A | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2609-1888T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777455 | ||||||
| chr19:16777463
|
G | A | 1 | a0004c0005t0018g0256 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2609-1880G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777463 | ||||||
| chr19:16777475
|
G | T | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1868G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777475 | ||||||
| chr19:16777541
|
A | T | 2 | a0001c0002t0007g0030a0001c0002t0011g0105 | 2 | HG02015.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2609-1802A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777541 | ||||||
| chr19:16777555
|
G | T | 1 | a0001c0002t0001g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2609-1788G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777555 | ||||||
| chr19:16777580
|
GGGAGGGG others(10): Show |
G | 16 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(13): Show | 16 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2609-1746_2609-173 others(21): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777580 | |||||
| chr19:16777604
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1739G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777604 | ||||||
| chr19:16777635
|
G | T | 1 | a0009c0028t0034g0258 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2609-1708G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777635 | ||||||
| chr19:16777644
|
A | G | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1699A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777644 | ||||||
| chr19:16777656
|
A | AG | 12 | a0001c0002t0002g0063a0002c0001t0005g0244a0002c0007t0001g0239others(9): Show | 12 | HG00280.hp1 HG00642.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2609-1683dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777656 | |||||
| chr19:16777663
|
A | G | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1680A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777663 | ||||||
| chr19:16777664
|
G | A | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1679G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777664 | ||||||
| chr19:16777665
|
C | G | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1678C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777665 | ||||||
| chr19:16777668
|
G | A | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1675G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777668 | ||||||
| chr19:16777671
|
A | G | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1672A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777671 | ||||||
| chr19:16777671
|
A | T | 1 | a0001c0002t0001g0142 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2609-1672A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777671 | ||||||
| chr19:16777684
|
G | A | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1659G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777684 | ||||||
| chr19:16777690
|
A | T | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1653A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777690 | ||||||
| chr19:16777694
|
GAGGGA | G | 4 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-1634_2609-163 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777694 | |||||
| chr19:16777741
|
G | A | 4 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-1602G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777741 | ||||||
| chr19:16777741
|
G | T | 1 | a0011c0011t0011g0025 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2609-1602G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777741 | ||||||
| chr19:16777755
|
A | T | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1588A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777755 | ||||||
| chr19:16777756
|
T | G | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1587T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777756 | ||||||
| chr19:16777806
|
A | T | 1 | a0001c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-1537A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777806 | ||||||
| chr19:16777807
|
A | C | 1 | a0001c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-1536A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777807 | ||||||
| chr19:16777903
|
AAG | A | 9 | a0009c0028t0002g0115a0009c0028t0034g0258a0009c0029t0002g0297others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2609-1439_2609-143 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16777903 | ||||||
| chr19:16777910
|
G | GGGGAAGG others(23): Show |
8 | a0001c0002t0001g0207a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG00673.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2609-1392_2609-136 others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777910 | |||||
| chr19:16777910
|
GGGGAAGG others(23): Show |
G | 2 | a0004c0009t0005g0140a0004c0009t0005g0224 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2609-1392_2609-136 others(34): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16777910 | |||||
| chr19:16778005
|
A | G | 1 | a0001c0002t0012g0203 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2609-1338A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778005 | ||||||
| chr19:16778045
|
G | T | 1 | a0002c0001t0005g0241 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2609-1298G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778045 | ||||||
| chr19:16778057
|
A | G | 1 | a0024c0036t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2609-1286A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778057 | ||||||
| chr19:16778062
|
A | G | 4 | a0020c0027t0007g0080a0039c0057t0026g0202a0041c0065t0032g0166others(1): Show | 4 | HG02083.hp1 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609-1281A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778062 | ||||||
| chr19:16778074
|
A | T | 1 | a0024c0036t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2609-1269A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778074 | ||||||
| chr19:16778076
|
C | A | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1267C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778076 | ||||||
| chr19:16778078
|
C | T | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1265C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778078 | ||||||
| chr19:16778094
|
G | C | 10 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(7): Show | 10 | HG02109.hp1 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.2609-1249G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778094 | ||||||
| chr19:16778100
|
G | T | 2 | a0001c0002t0005g0130a0002c0001t0005g0241 | 2 | NA18747.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.2609-1243G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778100 | ||||||
| chr19:16778153
|
C | A | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1190C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778153 | ||||||
| chr19:16778198
|
C | T | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1145C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778198 | ||||||
| chr19:16778199
|
C | T | 1 | a0010c0013t0013g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2609-1144C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778199 | ||||||
| chr19:16778210
|
C | T | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2609-1133C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778210 | ||||||
| chr19:16778253
|
G | A | 12 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(9): Show | 12 | HG02280.hp2 HG02647.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.2609-1090G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778253 | ||||||
| chr19:16778491
|
CTTCT | C | 7 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0157others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.2609-849_2609-846d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778491 | |||||
| chr19:16778494
|
C | CTTCTTTT others(5): Show |
1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2609-847_2609-846i others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | |||||
| chr19:16778494
|
C | CTTCTTTT others(6): Show |
3 | a0004c0005t0023g0094a0004c0005t0023g0095a0036c0048t0018g0129 | 3 | HG03490.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2609-847_2609-846i others(15): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | |||||
| chr19:16778494
|
C | CTTCTTTT others(7): Show |
17 | a0004c0005t0006g0211a0004c0005t0006g0225a0004c0005t0006g0228others(14): Show | 17 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2609-847_2609-846i others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | |||||
| chr19:16778494
|
C | CTTCTTTT others(8): Show |
10 | a0004c0005t0001g0296a0004c0005t0006g0226a0004c0060t0002g0125others(7): Show | 10 | HG01884.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2609-847_2609-846i others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | |||||
| chr19:16778494
|
C | CTTCTTTT others(9): Show |
2 | a0004c0005t0006g0227a0014c0054t0025g0118 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2609-847_2609-846i others(18): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | |||||
| chr19:16778494
|
CT | C | 183 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(180): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2609-835delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778494 | |||||
| chr19:16778497
|
T | C | 9 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(6): Show | 9 | HG02647.hp1 HG02809.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2609-846T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778497 | ||||||
| chr19:16778500
|
T | C | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2609-843T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778500 | ||||||
| chr19:16778506
|
T | G | 63 | a0001c0002t0003g0163a0001c0002t0004g0011a0001c0008t0001g0134others(60): Show | 63 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.2609-837T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778506 | ||||||
| chr19:16778506
|
TTTG | T | 16 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(13): Show | 16 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2609-818_2609-816d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16778506 | |||||
| chr19:16778508
|
TG | T | 6 | a0002c0001t0004g0108a0002c0001t0020g0289a0006c0044t0001g0255others(3): Show | 6 | HG00735.hp1 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2609-834delG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778508 | ||||||
| chr19:16778508
|
TGTTG | T | 9 | a0004c0009t0009g0052a0006c0014t0008g0253a0008c0010t0002g0114others(6): Show | 9 | HG02647.hp1 HG02809.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2609-834_2609-831d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778508 | ||||||
| chr19:16778509
|
G | T | 44 | a0001c0002t0001g0165a0004c0005t0001g0296a0004c0005t0006g0211others(41): Show | 44 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.2609-834G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778509 | ||||||
| chr19:16778512
|
G | T | 28 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(25): Show | 28 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.2609-831G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778512 | ||||||
| chr19:16778560
|
G | C | 1 | a0001c0002t0001g0189 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2609-783G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778560 | ||||||
| chr19:16778791
|
T | C | 299 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.2609-552T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778791 | ||||||
| chr19:16778800
|
A | G | 1 | a0039c0057t0026g0202 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2609-543A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778800 | ||||||
| chr19:16778801
|
C | A | 66 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(63): Show | 66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2609-542C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778801 | ||||||
| chr19:16778818
|
A | G | 1 | a0005c0004t0003g0272 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2609-525A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778818 | ||||||
| chr19:16778915
|
T | C | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2609-428T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778915 | ||||||
| chr19:16778916
|
G | A | 7 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(4): Show | 7 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2609-427G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16778916 | ||||||
| chr19:16779031
|
C | T | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2609-312C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779031 | ||||||
| chr19:16779063
|
G | A | 1 | a0026c0040t0002g0036 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2609-280G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779063 | ||||||
| chr19:16779092
|
C | G | 3 | a0001c0002t0001g0271a0003c0003t0002g0067a0003c0003t0002g0068 | 3 | HG02056.hp2 HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.2609-251C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779092 | ||||||
| chr19:16779340
|
C | T | 1 | a0006c0044t0001g0255 | 1 | NA19043.hp1 | splice_region_variant&intron_variant | LOW | c.2609-3C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 11/18 | chr19 | 16779340 | ||||||
| chr19:16779500
|
C | G | 33 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(30): Show | 33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2731+35C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779500 | ||||||
| chr19:16779510
|
A | G | 33 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(30): Show | 33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2731+45A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779510 | ||||||
| chr19:16779648
|
T | C | 12 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(9): Show | 12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+183T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779648 | ||||||
| chr19:16779764
|
G | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2731+299G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779764 | ||||||
| chr19:16779777
|
C | T | 20 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2731+312C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779777 | ||||||
| chr19:16779780
|
G | A | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2731+315G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779780 | ||||||
| chr19:16779835
|
T | C | 2 | a0001c0002t0003g0186a0005c0004t0004g0090 | 2 | NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2731+370T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779835 | ||||||
| chr19:16779946
|
C | T | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+481C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16779946 | ||||||
| chr19:16780099
|
C | T | 1 | a0003c0006t0002g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2731+634C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780099 | ||||||
| chr19:16780158
|
C | CT | 11 | a0001c0002t0001g0291a0002c0001t0003g0215a0002c0001t0014g0238others(8): Show | 11 | HG01257.hp2 HG01433.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.2731+708dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16780158 | |||||
| chr19:16780158
|
C | CTT | 9 | a0002c0001t0005g0184a0004c0060t0002g0125a0006c0044t0001g0255others(6): Show | 9 | HG01358.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2731+707_2731+708d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16780158 | |||||
| chr19:16780172
|
T | A | 2 | a0001c0002t0001g0208a0005c0004t0002g0059 | 2 | HG02129.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2731+707T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780172 | ||||||
| chr19:16780357
|
C | T | 12 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(9): Show | 12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+892C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780357 | ||||||
| chr19:16780378
|
A | G | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2731+913A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780378 | ||||||
| chr19:16780529
|
T | TCACATTC others(1): Show |
5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2731+1067_2731+107 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16780529 | |||||
| chr19:16780662
|
C | T | 84 | a0001c0022t0001g0151a0001c0022t0002g0102a0004c0005t0001g0296others(81): Show | 84 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.2731+1197C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16780662 | ||||||
| chr19:16781012
|
G | A | 12 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(9): Show | 12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+1547G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781012 | ||||||
| chr19:16781178
|
T | C | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+1713T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781178 | ||||||
| chr19:16781189
|
C | T | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+1724C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781189 | ||||||
| chr19:16781190
|
G | A | 33 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(30): Show | 33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2731+1725G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781190 | ||||||
| chr19:16781351
|
G | A | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.2731+1886G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781351 | ||||||
| chr19:16781547
|
T | C | 1 | a0003c0003t0004g0075 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2731+2082T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781547 | ||||||
| chr19:16781955
|
G | C | 1 | a0002c0001t0031g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2731+2490G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16781955 | ||||||
| chr19:16782084
|
A | G | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2731+2619A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782084 | ||||||
| chr19:16782093
|
C | CA | 8 | a0001c0002t0001g0191a0001c0002t0001g0201a0002c0001t0001g0242others(5): Show | 8 | HG00673.hp1 HG01943.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2731+2642dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782093 | |||||
| chr19:16782100
|
A | T | 12 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(9): Show | 12 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2731+2635A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782100 | ||||||
| chr19:16782108
|
G | A | 1 | a0002c0001t0003g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2731+2643G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782108 | ||||||
| chr19:16782108
|
GA | G | 15 | a0001c0002t0002g0010a0001c0022t0001g0151a0001c0022t0002g0102others(12): Show | 15 | HG00642.hp1 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2731+2654delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782108 | |||||
| chr19:16782284
|
T | TA | 35 | a0001c0002t0001g0291a0002c0001t0002g0029a0002c0001t0003g0183others(32): Show | 35 | HG00642.hp1 HG00735.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2731+2841dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | |||||
| chr19:16782284
|
T | TAA | 15 | a0004c0005t0023g0094a0004c0005t0023g0095a0004c0005t0039g0084others(12): Show | 15 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2731+2840_2731+284 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | |||||
| chr19:16782284
|
T | TAAA | 6 | a0008c0010t0047g0005a0012c0017t0002g0038a0026c0040t0002g0036others(3): Show | 6 | HG01361.hp1 HG02280.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2731+2839_2731+284 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | |||||
| chr19:16782284
|
TA | T | 18 | a0001c0002t0001g0191a0001c0002t0002g0031a0001c0002t0005g0192others(15): Show | 18 | HG00323.hp1 HG00673.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.2731+2841delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782284 | |||||
| chr19:16782333
|
G | A | 8 | a0006c0044t0001g0255a0008c0010t0002g0114a0008c0010t0010g0131others(5): Show | 8 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.2731+2868G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782333 | ||||||
| chr19:16782497
|
G | A | 4 | a0001c0002t0001g0199a0001c0002t0001g0268a0001c0002t0012g0188others(1): Show | 4 | HG02071.hp1 NA18945.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2731+3032G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782497 | ||||||
| chr19:16782526
|
A | G | 1 | a0044c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2731+3061A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782526 | ||||||
| chr19:16782558
|
TA | T | 3 | a0002c0001t0001g0260a0002c0001t0003g0195a0004c0005t0023g0095 | 3 | HG01943.hp1 HG03041.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.2731+3099delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782558 | |||||
| chr19:16782861
|
C | CTT | 66 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(63): Show | 66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2731+3397_2731+339 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782861 | |||||
| chr19:16782861
|
CTTCT | C | 98 | a0001c0002t0001g0142a0001c0002t0001g0148a0001c0002t0001g0153others(95): Show | 98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.2731+3417_2731+342 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782861 | |||||
| chr19:16782865
|
T | C | 66 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(63): Show | 66 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.2731+3400T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782865 | ||||||
| chr19:16782869
|
T | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2731+3404T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782869 | ||||||
| chr19:16782898
|
ATCCTTCC others(18): Show |
A | 67 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(64): Show | 67 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.2731+3448_2731+347 others(29): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16782898 | |||||
| chr19:16782912
|
CTTTCCTT others(9): Show |
C | 1 | a0014c0054t0025g0118 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2731+3448_2731+346 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16782912 | ||||||
| chr19:16783009
|
T | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2731+3544T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783009 | ||||||
| chr19:16783009
|
T | TTTCTTTC others(1): Show |
45 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(42): Show | 45 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(42): Show |
intron_variant | MODIFIER | c.2731+3552_2731+355 others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16783009 | |||||
| chr19:16783041
|
CT | C | 51 | a0002c0001t0004g0112a0004c0005t0001g0296a0004c0005t0006g0211others(48): Show | 51 | HG00642.hp2 HG01070.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.2731+3588delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16783041 | |||||
| chr19:16783234
|
C | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2731+3769C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783234 | ||||||
| chr19:16783279
|
C | G | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2731+3814C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783279 | ||||||
| chr19:16783360
|
A | C | 70 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(67): Show | 70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2731+3895A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783360 | ||||||
| chr19:16783469
|
T | C | 2 | a0013c0018t0017g0294a0013c0018t0017g0295 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2731+4004T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783469 | ||||||
| chr19:16783539
|
C | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2731+4074C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783539 | ||||||
| chr19:16783563
|
G | A | 1 | a0015c0020t0007g0119 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2731+4098G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783563 | ||||||
| chr19:16783590
|
C | T | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2731+4125C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783590 | ||||||
| chr19:16783591
|
G | T | 11 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2731+4126G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783591 | ||||||
| chr19:16783641
|
T | TA | 70 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(67): Show | 70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2731+4181dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16783641 | |||||
| chr19:16783643
|
A | G | 1 | a0001c0008t0001g0145 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2731+4178A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783643 | ||||||
| chr19:16783969
|
C | T | 4 | a0001c0022t0001g0151a0001c0022t0002g0102a0022c0042t0001g0152others(1): Show | 4 | HG01496.hp1 NA18993.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2731+4504C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783969 | ||||||
| chr19:16783970
|
G | A | 27 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(24): Show | 27 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.2731+4505G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783970 | ||||||
| chr19:16783977
|
C | T | 1 | a0002c0001t0003g0190 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2731+4512C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783977 | ||||||
| chr19:16783979
|
C | T | 23 | a0001c0002t0007g0030a0004c0009t0005g0140a0004c0009t0005g0224others(20): Show | 23 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.2731+4514C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16783979 | ||||||
| chr19:16784120
|
A | C | 1 | a0002c0007t0002g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2731+4655A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784120 | ||||||
| chr19:16784208
|
G | GA | 6 | a0001c0002t0001g0191a0001c0031t0001g0156a0002c0001t0001g0242others(3): Show | 6 | HG00673.hp1 HG01261.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2731+4756dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16784208 | |||||
| chr19:16784358
|
C | T | 70 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(67): Show | 70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-4624C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784358 | ||||||
| chr19:16784360
|
G | A | 1 | a0001c0035t0002g0020 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2732-4622G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784360 | ||||||
| chr19:16784449
|
G | A | 27 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(24): Show | 27 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.2732-4533G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784449 | ||||||
| chr19:16784536
|
G | A | 2 | a0007c0067t0003g0277a0009c0028t0034g0258 | 2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2732-4446G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784536 | ||||||
| chr19:16784668
|
C | T | 1 | a0003c0006t0002g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2732-4314C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784668 | ||||||
| chr19:16784856
|
G | C | 9 | a0001c0002t0001g0189a0001c0002t0001g0191a0001c0002t0001g0291others(6): Show | 9 | HG00673.hp1 NA18954.hp2 NA18963.hp1 others(6): Show |
intron_variant | MODIFIER | c.2732-4126G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16784856 | ||||||
| chr19:16784861
|
GGAGGTTG others(9): Show |
G | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-4117_2732-410 others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16784861 | |||||
| chr19:16785015
|
C | T | 2 | a0004c0005t0023g0094a0004c0005t0023g0095 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2732-3967C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785015 | ||||||
| chr19:16785127
|
G | T | 1 | a0001c0002t0001g0208 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2732-3855G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785127 | ||||||
| chr19:16785259
|
C | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-3723C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785259 | ||||||
| chr19:16785261
|
T | C | 139 | a0001c0002t0004g0011a0001c0008t0001g0145a0001c0008t0001g0168others(136): Show | 139 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.2732-3721T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785261 | ||||||
| chr19:16785282
|
C | CG | 3 | a0001c0008t0001g0168a0003c0059t0015g0037a0010c0013t0009g0045 | 3 | HG01175.hp1 HG01358.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2732-3697dupG | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785282 | |||||
| chr19:16785317
|
G | A | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-3665G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785317 | ||||||
| chr19:16785448
|
T | G | 1 | a0016c0019t0016g0004 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2732-3534T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785448 | ||||||
| chr19:16785513
|
AAAAAT | A | 5 | a0014c0025t0002g0048a0014c0025t0002g0049a0039c0057t0026g0202others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-3445_2732-344 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785513 | |||||
| chr19:16785584
|
ATGAC | A | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-3395_2732-339 others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785584 | |||||
| chr19:16785638
|
A | T | 1 | a0002c0001t0005g0155 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2732-3344A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785638 | ||||||
| chr19:16785769
|
AAC | A | 11 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2732-3211_2732-321 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785769 | |||||
| chr19:16785801
|
C | CTA | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-3171_2732-317 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16785801 | |||||
| chr19:16785867
|
A | T | 4 | a0012c0017t0001g0212a0012c0017t0002g0018a0012c0017t0002g0019others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2732-3115A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785867 | ||||||
| chr19:16785988
|
C | T | 2 | a0001c0002t0005g0192a0001c0002t0007g0041 | 2 | HG01975.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2732-2994C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16785988 | ||||||
| chr19:16786084
|
C | T | 11 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2732-2898C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786084 | ||||||
| chr19:16786131
|
T | C | 70 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(67): Show | 70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-2851T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786131 | ||||||
| chr19:16786181
|
CT | C | 70 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(67): Show | 70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-2791delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16786181 | |||||
| chr19:16786202
|
A | T | 75 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(72): Show | 75 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.2732-2780A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786202 | ||||||
| chr19:16786217
|
C | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-2765C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786217 | ||||||
| chr19:16786228
|
G | A | 4 | a0001c0008t0001g0135a0001c0008t0001g0139a0001c0008t0002g0044others(1): Show | 4 | NA18982.hp2 NA19007.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-2754G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786228 | ||||||
| chr19:16786266
|
T | C | 70 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(67): Show | 70 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.2732-2716T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786266 | ||||||
| chr19:16786267
|
G | A | 1 | a0002c0001t0031g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2732-2715G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786267 | ||||||
| chr19:16786553
|
C | CT | 69 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(66): Show | 69 | HG00642.hp2 HG00735.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.2732-2418dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16786553 | |||||
| chr19:16786635
|
T | C | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-2347T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786635 | ||||||
| chr19:16786692
|
G | A | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-2290G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786692 | ||||||
| chr19:16786747
|
T | G | 1 | a0004c0005t0039g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2732-2235T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786747 | ||||||
| chr19:16786774
|
A | T | 1 | a0001c0002t0001g0191 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2732-2208A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786774 | ||||||
| chr19:16786854
|
G | A | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-2128G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786854 | ||||||
| chr19:16786894
|
G | A | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2732-2088G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16786894 | ||||||
| chr19:16787093
|
G | A | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2732-1889G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787093 | ||||||
| chr19:16787368
|
G | A | 1 | a0011c0011t0002g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2732-1614G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787368 | ||||||
| chr19:16787626
|
G | A | 4 | a0009c0069t0043g0299a0039c0057t0026g0202a0041c0065t0032g0166others(1): Show | 4 | HG02818.hp1 HG02922.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-1356G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787626 | ||||||
| chr19:16787870
|
TAATAAC | T | 7 | a0001c0002t0005g0130a0002c0001t0001g0171a0002c0001t0005g0184others(4): Show | 7 | HG01358.hp1 HG01433.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.2732-1106_2732-110 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787870 | |||||
| chr19:16787876
|
C | A | 34 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(31): Show | 34 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.2732-1106C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787876 | ||||||
| chr19:16787876
|
C | T | 11 | a0001c0002t0005g0192a0001c0002t0007g0041a0004c0005t0029g0265others(8): Show | 11 | HG01361.hp1 HG01975.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.2732-1106C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787876 | ||||||
| chr19:16787876
|
CAAT | C | 39 | a0001c0002t0003g0186a0001c0002t0004g0011a0001c0008t0001g0270others(36): Show | 39 | HG00099.hp1 HG00597.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.2732-1078_2732-107 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787876 | |||||
| chr19:16787876
|
CAATAAT | C | 6 | a0001c0008t0002g0044a0002c0001t0003g0236a0003c0003t0004g0079others(3): Show | 6 | HG01884.hp2 HG01943.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.2732-1081_2732-107 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787876 | |||||
| chr19:16787898
|
AATAATAA others(14): Show |
A | 2 | a0004c0005t0022g0050a0033c0052t0001g0254 | 2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2732-1081_2732-106 others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787898 | |||||
| chr19:16787898
|
AATAATAA others(17): Show |
A | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2732-1081_2732-105 others(28): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787898 | |||||
| chr19:16787901
|
A | C | 5 | a0002c0001t0001g0160a0002c0001t0003g0176a0002c0001t0005g0241others(2): Show | 5 | HG01109.hp1 HG01361.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-1081A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787901 | ||||||
| chr19:16787901
|
AATAATC | A | 7 | a0001c0008t0001g0134a0001c0008t0001g0135a0001c0008t0001g0139others(4): Show | 7 | HG02129.hp1 HG02572.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.2732-1078_2732-107 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | |||||
| chr19:16787901
|
AATAATCA others(2): Show |
A | 5 | a0001c0002t0001g0153a0001c0002t0005g0192a0001c0002t0020g0249others(2): Show | 5 | HG01099.hp2 HG02293.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2732-1078_2732-107 others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | |||||
| chr19:16787901
|
AATAATCA others(5): Show |
A | 1 | a0004c0005t0006g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2732-1078_2732-106 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | |||||
| chr19:16787901
|
AATAATCA others(17): Show |
A | 1 | a0008c0010t0002g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2732-1078_2732-105 others(28): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787901 | |||||
| chr19:16787904
|
A | C | 21 | a0001c0002t0004g0011a0001c0002t0005g0130a0002c0001t0001g0160others(18): Show | 21 | HG00099.hp1 HG00738.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.2732-1078A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787904 | ||||||
| chr19:16787904
|
AATC | A | 76 | a0001c0002t0001g0175a0001c0002t0001g0181a0001c0002t0001g0189others(73): Show | 76 | HG00280.hp1 HG00597.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2732-1039_2732-103 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787904
|
AATCATC | A | 65 | a0001c0002t0001g0142a0001c0002t0001g0148a0001c0002t0001g0170others(62): Show | 65 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.2732-1042_2732-103 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787904
|
AATCATCA others(2): Show |
A | 33 | a0001c0002t0001g0146a0001c0002t0001g0154a0001c0002t0001g0157others(30): Show | 33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.2732-1045_2732-103 others(13): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787904
|
AATCATCA others(5): Show |
A | 4 | a0004c0005t0018g0256a0009c0068t0040g0116a0009c0069t0043g0299others(1): Show | 4 | HG02258.hp1 HG02896.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-1048_2732-103 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787904
|
AATCATCA others(8): Show |
A | 11 | a0004c0005t0006g0211a0004c0005t0006g0227a0004c0005t0006g0228others(8): Show | 11 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2732-1051_2732-103 others(19): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787904
|
AATCATCA others(11): Show |
A | 4 | a0008c0010t0010g0131a0008c0010t0010g0276a0008c0010t0010g0278others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2732-1054_2732-103 others(22): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787904
|
AATCATCA others(14): Show |
A | 2 | a0004c0060t0002g0125a0026c0040t0002g0036 | 2 | HG01361.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2732-1057_2732-103 others(25): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787904
|
AATCATCA others(17): Show |
A | 2 | a0004c0005t0029g0265a0006c0044t0001g0255 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2732-1060_2732-103 others(28): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16787904 | |||||
| chr19:16787907
|
C | A | 25 | a0001c0002t0001g0196a0001c0002t0001g0218a0002c0001t0001g0171others(22): Show | 25 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2732-1075C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787907 | ||||||
| chr19:16787910
|
C | A | 64 | a0001c0002t0001g0175a0001c0002t0001g0181a0001c0002t0001g0189others(61): Show | 64 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.2732-1072C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787910 | ||||||
| chr19:16787913
|
C | A | 87 | a0001c0002t0001g0142a0001c0002t0001g0148a0001c0002t0001g0170others(84): Show | 87 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.2732-1069C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787913 | ||||||
| chr19:16787916
|
C | A | 82 | a0001c0002t0001g0146a0001c0002t0001g0154a0001c0002t0001g0157others(79): Show | 82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.2732-1066C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787916 | ||||||
| chr19:16787919
|
C | A | 43 | a0001c0002t0001g0154a0001c0002t0001g0175a0001c0002t0001g0189others(40): Show | 43 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.2732-1063C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787919 | ||||||
| chr19:16787922
|
C | A | 16 | a0001c0002t0001g0189a0001c0002t0001g0191a0001c0002t0001g0193others(13): Show | 16 | HG00642.hp2 HG00673.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2732-1060C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787922 | ||||||
| chr19:16787925
|
C | A | 8 | a0001c0002t0001g0191a0001c0002t0001g0193a0002c0001t0001g0180others(5): Show | 8 | HG00642.hp2 HG00673.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2732-1057C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787925 | ||||||
| chr19:16787928
|
C | A | 3 | a0004c0005t0023g0094a0004c0005t0023g0095a0004c0060t0002g0125 | 3 | HG02886.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2732-1054C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787928 | ||||||
| chr19:16787995
|
G | A | 1 | a0009c0069t0043g0299 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2732-987G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16787995 | ||||||
| chr19:16788186
|
C | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-796C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788186 | ||||||
| chr19:16788232
|
A | AAAT | 5 | a0001c0002t0001g0196a0001c0002t0001g0207a0001c0002t0012g0178others(2): Show | 5 | HG00673.hp2 HG02083.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-699_2732-697d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788232
|
AAAT | A | 107 | a0001c0002t0001g0146a0001c0002t0001g0148a0001c0002t0001g0153others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.2732-699_2732-697d others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788232
|
AAATAAT | A | 50 | a0001c0002t0001g0271a0001c0002t0003g0144a0001c0002t0003g0200others(47): Show | 50 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.2732-702_2732-697d others(8): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788232
|
AAATAATA others(2): Show |
A | 39 | a0001c0002t0001g0291a0001c0022t0001g0151a0003c0003t0003g0288others(36): Show | 39 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.2732-705_2732-697d others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788232
|
AAATAATA others(5): Show |
A | 7 | a0004c0005t0018g0256a0006c0014t0009g0014a0012c0017t0001g0212others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2732-708_2732-697d others(14): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788232
|
AAATAATA others(8): Show |
A | 12 | a0004c0005t0001g0296a0004c0060t0002g0125a0009c0028t0002g0115others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2732-711_2732-697d others(17): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788232
|
AAATAATA others(11): Show |
A | 1 | a0001c0022t0002g0102 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2732-714_2732-697d others(20): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788232
|
AAATAATA others(14): Show |
A | 4 | a0011c0011t0002g0022a0011c0011t0011g0017a0011c0011t0011g0024others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.2732-717_2732-697d others(23): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788232 | |||||
| chr19:16788270
|
A | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2732-712A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788270 | ||||||
| chr19:16788284
|
A | G | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2732-698A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788284 | ||||||
| chr19:16788396
|
C | T | 1 | a0012c0017t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2732-586C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788396 | ||||||
| chr19:16788467
|
G | C | 3 | a0001c0022t0001g0151a0001c0022t0002g0102a0022c0042t0001g0152 | 3 | HG01496.hp1 NA18993.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2732-515G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788467 | ||||||
| chr19:16788533
|
C | G | 1 | a0003c0006t0002g0100 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2732-449C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788533 | ||||||
| chr19:16788564
|
C | CA | 65 | a0001c0002t0001g0157a0001c0002t0001g0271a0001c0002t0020g0249others(62): Show | 65 | HG00099.hp2 HG00642.hp2 HG01081.hp1 others(62): Show |
intron_variant | MODIFIER | c.2732-399dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788564 | |||||
| chr19:16788564
|
CA | C | 16 | a0001c0002t0002g0010a0001c0002t0003g0144a0001c0002t0004g0033others(13): Show | 16 | HG01070.hp2 HG01256.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2732-399delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16788564 | |||||
| chr19:16788920
|
A | G | 86 | a0001c0022t0001g0151a0001c0022t0002g0102a0004c0005t0001g0296others(83): Show | 86 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(83): Show |
intron_variant | MODIFIER | c.2732-62A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 12/18 | chr19 | 16788920 | ||||||
| chr19:16789368
|
C | T | 3 | a0001c0008t0001g0270a0003c0006t0002g0086a0003c0006t0002g0096 | 3 | HG00733.hp1 HG00738.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.2940+178C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16789368 | ||||||
| chr19:16789716
|
C | CT | 62 | a0001c0008t0001g0145a0001c0008t0001g0168a0001c0008t0001g0270others(59): Show | 62 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.2940+545dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16789716 | |||||
| chr19:16789716
|
C | CTT | 28 | a0002c0047t0001g0138a0004c0005t0001g0296a0004c0005t0006g0211others(25): Show | 28 | HG00642.hp2 HG01081.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.2940+544_2940+545d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16789716 | |||||
| chr19:16789716
|
CT | C | 10 | a0001c0002t0002g0010a0001c0002t0012g0198a0002c0001t0004g0107others(7): Show | 10 | HG01081.hp2 HG02040.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2940+545delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16789716 | |||||
| chr19:16789757
|
G | A | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2940+567G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16789757 | ||||||
| chr19:16789855
|
C | T | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2940+665C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16789855 | ||||||
| chr19:16790009
|
T | C | 11 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2940+819T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790009 | ||||||
| chr19:16790067
|
G | A | 129 | a0001c0008t0001g0145a0001c0008t0001g0168a0001c0008t0001g0270others(126): Show | 129 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(126): Show |
intron_variant | MODIFIER | c.2940+877G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790067 | ||||||
| chr19:16790356
|
G | A | 1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2941-994G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790356 | ||||||
| chr19:16790372
|
G | A | 1 | a0008c0010t0002g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2941-978G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790372 | ||||||
| chr19:16790469
|
T | C | 1 | a0010c0013t0008g0194 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2941-881T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790469 | ||||||
| chr19:16790471
|
G | A | 1 | a0002c0001t0020g0289 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2941-879G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790471 | ||||||
| chr19:16790472
|
G | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2941-878G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790472 | ||||||
| chr19:16790491
|
C | A | 1 | a0003c0003t0002g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2941-859C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790491 | ||||||
| chr19:16790636
|
AAAAAATA others(3): Show |
A | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2941-710_2941-701d others(12): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790636 | |||||
| chr19:16790638
|
A | AAATAATA others(2): Show |
5 | a0014c0025t0002g0048a0014c0025t0002g0049a0039c0057t0026g0202others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2941-710_2941-709i others(11): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790638 | |||||
| chr19:16790639
|
A | AAAAT | 146 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(143): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.2941-709_2941-708i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790639 | |||||
| chr19:16790639
|
A | ATAAT | 6 | a0002c0007t0049g0132a0003c0006t0002g0071a0003c0006t0002g0100others(3): Show | 6 | HG01884.hp2 HG01981.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2941-711_2941-710i others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790639 | ||||||
| chr19:16790640
|
A | T | 21 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.2941-710A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790640 | ||||||
| chr19:16790641
|
AT | A | 7 | a0002c0001t0004g0035a0003c0003t0003g0143a0003c0003t0004g0026others(4): Show | 7 | HG00280.hp1 HG01257.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.2941-708delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790641 | ||||||
| chr19:16790642
|
T | A | 42 | a0001c0002t0001g0189a0001c0002t0001g0191a0001c0002t0001g0291others(39): Show | 42 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.2941-708T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790642 | ||||||
| chr19:16790643
|
A | T | 34 | a0001c0002t0001g0189a0001c0002t0001g0191a0001c0002t0001g0291others(31): Show | 34 | HG00639.hp1 HG00673.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2941-707A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790643 | ||||||
| chr19:16790646
|
T | A | 9 | a0002c0001t0004g0032a0002c0001t0004g0034a0002c0001t0004g0035others(6): Show | 9 | HG00280.hp1 HG01257.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2941-704T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790646 | ||||||
| chr19:16790652
|
AAT | A | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2941-696_2941-695d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16790652 | |||||
| chr19:16790655
|
A | T | 43 | a0004c0005t0001g0296a0004c0005t0006g0211a0004c0005t0006g0225others(40): Show | 43 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(40): Show |
intron_variant | MODIFIER | c.2941-695A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790655 | ||||||
| chr19:16790743
|
C | T | 22 | a0004c0009t0005g0140a0004c0009t0005g0224a0004c0009t0008g0205others(19): Show | 22 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2941-607C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790743 | ||||||
| chr19:16790794
|
G | T | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2941-556G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790794 | ||||||
| chr19:16790950
|
G | A | 1 | a0006c0014t0002g0015 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2941-400G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790950 | ||||||
| chr19:16790999
|
A | G | 2 | a0002c0007t0001g0217a0003c0006t0002g0061 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2941-351A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 13/18 | chr19 | 16790999 | ||||||
| chr19:16791813
|
A | G | 11 | a0001c0022t0001g0151a0001c0022t0002g0102a0009c0028t0002g0115others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.3213+191A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16791813 | ||||||
| chr19:16791954
|
T | C | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3213+332T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16791954 | ||||||
| chr19:16792276
|
C | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3213+654C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792276 | ||||||
| chr19:16792299
|
G | A | 2 | a0016c0019t0016g0003a0016c0019t0016g0004 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3213+677G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792299 | ||||||
| chr19:16792360
|
G | A | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3213+738G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792360 | ||||||
| chr19:16792443
|
G | A | 11 | a0003c0003t0003g0143a0003c0003t0004g0026a0003c0003t0004g0075others(8): Show | 11 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.3213+821G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792443 | ||||||
| chr19:16792479
|
C | G | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3213+857C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792479 | ||||||
| chr19:16792526
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3213+904C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792526 | ||||||
| chr19:16792539
|
G | A | 1 | a0012c0017t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3213+917G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792539 | ||||||
| chr19:16792635
|
T | C | 3 | a0001c0002t0003g0144a0001c0002t0003g0163a0002c0001t0003g0162 | 3 | HG01256.hp2 HG01346.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.3213+1013T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792635 | ||||||
| chr19:16792734
|
G | A | 1 | a0003c0003t0002g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3213+1112G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792734 | ||||||
| chr19:16792791
|
C | A | 1 | a0003c0006t0002g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3213+1169C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16792791 | ||||||
| chr19:16792876
|
C | CA | 31 | a0001c0002t0001g0199a0001c0008t0001g0145a0002c0001t0003g0176others(28): Show | 31 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.3213+1273dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16792876 | |||||
| chr19:16792876
|
CA | C | 27 | a0001c0002t0005g0130a0001c0008t0027g0136a0001c0022t0001g0151others(24): Show | 27 | HG00558.hp1 HG01074.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.3213+1273delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16792876 | |||||
| chr19:16793060
|
TA | T | 174 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.3214-1392delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16793060 | |||||
| chr19:16793176
|
C | T | 3 | a0002c0001t0005g0155a0002c0001t0005g0245a0002c0001t0014g0187 | 3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.3214-1287C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793176 | ||||||
| chr19:16793250
|
T | C | 1 | a0002c0001t0002g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3214-1213T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793250 | ||||||
| chr19:16793583
|
GT | G | 199 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.3214-869delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16793583 | |||||
| chr19:16793738
|
G | A | 20 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3214-725G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793738 | ||||||
| chr19:16793806
|
A | G | 2 | a0002c0001t0005g0155a0002c0001t0014g0187 | 2 | HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.3214-657A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793806 | ||||||
| chr19:16793813
|
G | A | 1 | a0002c0007t0002g0057 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3214-650G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793813 | ||||||
| chr19:16793975
|
T | C | 3 | a0039c0057t0026g0202a0041c0065t0032g0166a0042c0066t0008g0264 | 3 | HG02818.hp1 HG02922.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3214-488T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16793975 | ||||||
| chr19:16794049
|
A | G | 40 | a0001c0008t0001g0145a0001c0008t0001g0168a0001c0008t0001g0270others(37): Show | 40 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.3214-414A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794049 | ||||||
| chr19:16794120
|
C | T | 2 | a0001c0002t0003g0186a0005c0004t0004g0090 | 2 | NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.3214-343C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794120 | ||||||
| chr19:16794183
|
T | C | 1 | a0017c0021t0001g0231 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3214-280T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794183 | ||||||
| chr19:16794290
|
C | T | 32 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(29): Show | 32 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(29): Show |
intron_variant | MODIFIER | c.3214-173C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794290 | ||||||
| chr19:16794412
|
G | A | 1 | a0044c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3214-51G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 14/18 | chr19 | 16794412 | ||||||
| chr19:16794644
|
A | C | 41 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0191others(38): Show | 41 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.3304+91A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794644 | ||||||
| chr19:16794663
|
G | T | 299 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.3304+110G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794663 | ||||||
| chr19:16794714
|
C | T | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3304+161C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794714 | ||||||
| chr19:16794716
|
A | T | 81 | a0001c0022t0001g0151a0001c0022t0002g0102a0004c0005t0001g0296others(78): Show | 81 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.3304+163A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794716 | ||||||
| chr19:16794800
|
T | G | 125 | a0001c0002t0001g0189a0001c0008t0001g0145a0001c0008t0001g0168others(122): Show | 125 | HG00099.hp1 HG00639.hp1 HG00642.hp2 others(122): Show |
intron_variant | MODIFIER | c.3304+247T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794800 | ||||||
| chr19:16794896
|
G | A | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3304+343G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794896 | ||||||
| chr19:16794931
|
A | G | 1 | a0003c0003t0007g0064 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3304+378A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16794931 | ||||||
| chr19:16795076
|
G | A | 2 | a0002c0001t0001g0197a0004c0060t0002g0125 | 2 | HG02886.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.3304+523G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795076 | ||||||
| chr19:16795217
|
G | A | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3304+664G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795217 | ||||||
| chr19:16795318
|
G | A | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3304+765G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795318 | ||||||
| chr19:16795395
|
T | A | 4 | a0008c0010t0010g0131a0008c0010t0010g0276a0008c0010t0010g0278others(1): Show | 4 | HG02647.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3304+842T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795395 | ||||||
| chr19:16795415
|
C | CT | 36 | a0001c0008t0001g0168a0002c0001t0001g0147a0002c0001t0001g0171others(33): Show | 36 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.3304+881dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16795415 | |||||
| chr19:16795415
|
CT | C | 18 | a0001c0002t0012g0178a0002c0001t0005g0241a0002c0001t0033g0216others(15): Show | 18 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.3304+881delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16795415 | |||||
| chr19:16795415
|
CTTTT | C | 8 | a0008c0010t0002g0114a0008c0010t0010g0131a0008c0010t0010g0276others(5): Show | 8 | HG01361.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3304+878_3304+881d others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16795415 | |||||
| chr19:16795519
|
C | T | 1 | a0002c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3304+966C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795519 | ||||||
| chr19:16795573
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3304+1020C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795573 | ||||||
| chr19:16795579
|
G | A | 1 | a0008c0010t0010g0284 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3304+1026G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16795579 | ||||||
| chr19:16796560
|
T | C | 25 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3305-1172T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796560 | ||||||
| chr19:16796570
|
T | C | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3305-1162T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796570 | ||||||
| chr19:16796588
|
T | C | 30 | a0001c0022t0001g0151a0001c0022t0002g0102a0004c0005t0006g0211others(27): Show | 30 | HG01496.hp1 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.3305-1144T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796588 | ||||||
| chr19:16796605
|
G | A | 21 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.3305-1127G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796605 | ||||||
| chr19:16796677
|
C | T | 45 | a0001c0002t0001g0189a0001c0002t0004g0011a0001c0008t0001g0168others(42): Show | 45 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.3305-1055C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796677 | ||||||
| chr19:16796696
|
C | CTTT | 25 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3305-1034_3305-103 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16796696 | |||||
| chr19:16796765
|
G | A | 14 | a0001c0022t0001g0151a0001c0022t0002g0102a0005c0004t0001g0274others(11): Show | 14 | HG01496.hp1 HG01891.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3305-967G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16796765 | ||||||
| chr19:16797125
|
A | G | 2 | a0004c0009t0008g0205a0004c0009t0036g0126 | 2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3305-607A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797125 | ||||||
| chr19:16797194
|
AT | A | 5 | a0004c0005t0023g0094a0004c0005t0023g0095a0004c0005t0039g0084others(2): Show | 5 | HG00642.hp2 HG01081.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.3305-536delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16797194 | |||||
| chr19:16797197
|
G | C | 3 | a0017c0021t0001g0231a0017c0021t0002g0046a0017c0021t0002g0051 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3305-535G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797197 | ||||||
| chr19:16797290
|
C | G | 1 | a0034c0051t0002g0028 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3305-442C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797290 | ||||||
| chr19:16797324
|
ATC | A | 20 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.3305-404_3305-403d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16797324 | |||||
| chr19:16797328
|
C | CT | 34 | a0001c0002t0001g0170a0001c0002t0001g0179a0001c0002t0001g0218others(31): Show | 34 | HG00609.hp1 HG01175.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.3305-384dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr19 | 16797328 | |||||
| chr19:16797372
|
C | A | 1 | a0024c0036t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3305-360C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797372 | ||||||
| chr19:16797555
|
C | T | 8 | a0001c0002t0001g0146a0001c0002t0001g0153a0001c0002t0001g0154others(5): Show | 8 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(5): Show |
intron_variant | MODIFIER | c.3305-177C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 15/18 | chr19 | 16797555 | ||||||
| chr19:16798156
|
T | G | 2 | a0004c0009t0013g0206a0006c0014t0002g0015 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3459+270T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798156 | ||||||
| chr19:16798268
|
CT | C | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3459+389delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr19 | 16798268 | |||||
| chr19:16798364
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3459+478C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798364 | ||||||
| chr19:16798431
|
A | G | 27 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(24): Show | 27 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.3459+545A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798431 | ||||||
| chr19:16798467
|
C | G | 1 | a0001c0002t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3459+581C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798467 | ||||||
| chr19:16798479
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3459+593C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798479 | ||||||
| chr19:16798708
|
C | T | 2 | a0007c0012t0001g0234a0007c0012t0001g0235 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3459+822C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798708 | ||||||
| chr19:16798903
|
G | A | 3 | a0017c0021t0001g0231a0017c0021t0002g0046a0017c0021t0002g0051 | 3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3460-983G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798903 | ||||||
| chr19:16798939
|
T | TA | 78 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(75): Show | 78 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.3460-934dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr19 | 16798939 | |||||
| chr19:16798940
|
A | T | 1 | a0003c0006t0038g0106 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3460-946A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798940 | ||||||
| chr19:16798950
|
A | AC | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3460-936_3460-935i others(3): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16798950 | ||||||
| chr19:16799256
|
C | T | 1 | a0020c0027t0007g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3460-630C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799256 | ||||||
| chr19:16799528
|
C | T | 31 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(28): Show | 31 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3460-358C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799528 | ||||||
| chr19:16799663
|
A | C | 27 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(24): Show | 27 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.3460-223A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799663 | ||||||
| chr19:16799664
|
G | A | 25 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-222G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799664 | ||||||
| chr19:16799667
|
T | C | 25 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-219T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799667 | ||||||
| chr19:16799668
|
G | A | 25 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-218G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799668 | ||||||
| chr19:16799669
|
G | A | 25 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-217G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799669 | ||||||
| chr19:16799675
|
T | A | 25 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3460-211T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799675 | ||||||
| chr19:16799727
|
C | T | 1 | a0022c0042t0001g0152 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3460-159C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799727 | ||||||
| chr19:16799734
|
C | A | 1 | a0001c0002t0005g0192 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3460-152C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 16/18 | chr19 | 16799734 | ||||||
| chr19:16800178
|
G | A | 4 | a0009c0069t0043g0299a0013c0018t0017g0294a0013c0018t0017g0295others(1): Show | 4 | HG03098.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3736+16G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800178 | ||||||
| chr19:16800390
|
C | T | 1 | a0001c0002t0002g0007 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.3736+228C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800390 | ||||||
| chr19:16800426
|
T | C | 1 | a0001c0002t0002g0063 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3736+264T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800426 | ||||||
| chr19:16800439
|
C | CAGG | 210 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0148others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.3736+279_3736+280i others(5): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16800439 | |||||
| chr19:16800479
|
C | T | 3 | a0001c0002t0001g0271a0002c0001t0001g0180a0003c0003t0002g0068 | 3 | HG02056.hp2 HG02080.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3736+317C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800479 | ||||||
| chr19:16800500
|
C | T | 21 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.3736+338C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800500 | ||||||
| chr19:16800505
|
T | G | 1 | a0003c0003t0002g0065 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3736+343T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800505 | ||||||
| chr19:16800863
|
G | T | 2 | a0006c0014t0009g0014a0006c0014t0009g0016 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3736+701G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800863 | ||||||
| chr19:16800901
|
G | A | 3 | a0002c0001t0001g0260a0002c0001t0001g0262a0005c0004t0002g0039 | 3 | HG01167.hp2 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3736+739G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16800901 | ||||||
| chr19:16801067
|
C | T | 2 | a0002c0001t0001g0261a0040c0056t0001g0279 | 2 | HG01167.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.3736+905C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801067 | ||||||
| chr19:16801589
|
A | G | 84 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(81): Show | 84 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.3736+1427A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801589 | ||||||
| chr19:16801862
|
A | T | 136 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0189others(133): Show | 136 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.3736+1700A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801862 | ||||||
| chr19:16801879
|
C | T | 1 | a0006c0015t0028g0204 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3736+1717C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801879 | ||||||
| chr19:16801904
|
C | T | 15 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(12): Show | 15 | HG00609.hp2 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3736+1742C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16801904 | ||||||
| chr19:16802234
|
T | C | 4 | a0009c0069t0043g0299a0013c0018t0017g0294a0013c0018t0017g0295others(1): Show | 4 | HG03098.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3736+2072T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802234 | ||||||
| chr19:16802286
|
T | TAAATAAA others(5): Show |
49 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0189others(46): Show | 49 | HG00099.hp1 HG00544.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.3736+2137_3736+214 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802286 | |||||
| chr19:16802323
|
G | A | 21 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.3736+2161G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802323 | ||||||
| chr19:16802374
|
C | T | 66 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0153others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.3736+2212C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802374 | ||||||
| chr19:16802410
|
T | C | 43 | a0001c0002t0001g0146a0001c0002t0001g0153a0001c0002t0001g0154others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.3736+2248T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802410 | ||||||
| chr19:16802451
|
C | A | 31 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(28): Show | 31 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3736+2289C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802451 | ||||||
| chr19:16802463
|
TA | T | 93 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0179others(90): Show | 93 | HG00323.hp1 HG00544.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.3736+2323delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802463 | |||||
| chr19:16802463
|
TAA | T | 18 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(15): Show | 18 | HG00099.hp1 HG00609.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.3736+2322_3736+232 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802463 | |||||
| chr19:16802547
|
C | T | 6 | a0002c0046t0001g0219a0003c0006t0001g0128a0003c0059t0015g0037others(3): Show | 6 | HG00099.hp1 HG01074.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.3736+2385C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802547 | ||||||
| chr19:16802605
|
T | G | 1 | a0004c0005t0006g0226 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3736+2443T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802605 | ||||||
| chr19:16802943
|
G | A | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3736+2781G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16802943 | ||||||
| chr19:16802947
|
C | CA | 10 | a0001c0002t0001g0271a0001c0002t0020g0249a0002c0001t0003g0183others(7): Show | 10 | HG01099.hp2 HG02080.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.3736+2803dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802947 | |||||
| chr19:16802947
|
C | CAA | 21 | a0004c0005t0006g0211a0004c0005t0006g0225a0004c0005t0006g0226others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.3736+2802_3736+280 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802947 | |||||
| chr19:16802947
|
C | CAAA | 15 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(12): Show | 15 | HG00609.hp2 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.3736+2801_3736+280 others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16802947 | |||||
| chr19:16803076
|
T | C | 1 | a0003c0003t0002g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3736+2914T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803076 | ||||||
| chr19:16803105
|
G | A | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3736+2943G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803105 | ||||||
| chr19:16803109
|
G | A | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3736+2947G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803109 | ||||||
| chr19:16803151
|
G | A | 66 | a0001c0002t0001g0142a0001c0002t0001g0146a0001c0002t0001g0153others(63): Show | 66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.3736+2989G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803151 | ||||||
| chr19:16803336
|
A | G | 1 | a0019c0024t0001g0251 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3736+3174A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803336 | ||||||
| chr19:16803623
|
C | G | 31 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(28): Show | 31 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.3736+3461C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803623 | ||||||
| chr19:16803639
|
A | G | 33 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(30): Show | 33 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.3736+3477A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803639 | ||||||
| chr19:16803692
|
G | A | 1 | a0001c0002t0002g0031 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3736+3530G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16803692 | ||||||
| chr19:16803755
|
T | TA | 14 | a0001c0002t0002g0007a0001c0031t0001g0156a0002c0001t0004g0113others(11): Show | 14 | HG01261.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3736+3613dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16803755 | |||||
| chr19:16803755
|
TA | T | 26 | a0001c0002t0001g0154a0001c0002t0001g0165a0001c0002t0005g0192others(23): Show | 26 | HG00280.hp2 HG01099.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.3736+3613delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16803755 | |||||
| chr19:16803927
|
G | GA | 6 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(3): Show | 6 | HG00609.hp2 HG01496.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.3737-3649dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16803927 | |||||
| chr19:16804019
|
G | A | 2 | a0004c0009t0013g0206a0006c0014t0002g0015 | 2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3737-3567G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804019 | ||||||
| chr19:16804141
|
C | T | 46 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(43): Show | 46 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3737-3445C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804141 | ||||||
| chr19:16804182
|
C | A | 1 | a0024c0036t0001g0209 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3737-3404C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804182 | ||||||
| chr19:16804370
|
C | G | 17 | a0001c0002t0003g0186a0001c0002t0004g0011a0002c0001t0003g0176others(14): Show | 17 | HG00597.hp2 HG01081.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3737-3216C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804370 | ||||||
| chr19:16804518
|
C | T | 19 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(16): Show | 19 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.3737-3068C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804518 | ||||||
| chr19:16804554
|
C | T | 46 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(43): Show | 46 | HG00642.hp2 HG00735.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.3737-3032C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804554 | ||||||
| chr19:16804575
|
A | G | 3 | a0001c0031t0001g0156a0003c0006t0001g0281a0003c0006t0001g0282 | 3 | HG02698.hp1 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.3737-3011A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804575 | ||||||
| chr19:16804594
|
G | GTTTTT | 18 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(15): Show | 18 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.3737-2985_3737-298 others(9): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16804594 | |||||
| chr19:16804605
|
T | A | 1 | a0004c0005t0022g0050 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3737-2981T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804605 | ||||||
| chr19:16804649
|
G | A | 2 | a0014c0025t0002g0048a0014c0025t0002g0049 | 2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3737-2937G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804649 | ||||||
| chr19:16804754
|
G | A | 1 | a0002c0001t0002g0043 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3737-2832G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804754 | ||||||
| chr19:16804816
|
CT | C | 72 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(69): Show | 72 | HG00609.hp2 HG00642.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.3737-2762delT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16804816 | |||||
| chr19:16804894
|
G | A | 1 | a0003c0006t0002g0071 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3737-2692G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804894 | ||||||
| chr19:16804981
|
C | T | 5 | a0011c0011t0001g0247a0011c0011t0002g0022a0011c0011t0011g0017others(2): Show | 5 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3737-2605C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16804981 | ||||||
| chr19:16805020
|
T | C | 1 | a0008c0010t0002g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3737-2566T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805020 | ||||||
| chr19:16805328
|
G | A | 19 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(16): Show | 19 | HG00609.hp2 HG01496.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.3737-2258G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805328 | ||||||
| chr19:16805330
|
A | G | 9 | a0006c0044t0001g0255a0008c0010t0002g0114a0008c0010t0010g0131others(6): Show | 9 | HG01361.hp1 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.3737-2256A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805330 | ||||||
| chr19:16805667
|
A | G | 1 | a0004c0009t0009g0047 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3737-1919A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805667 | ||||||
| chr19:16805873
|
C | CT | 6 | a0004c0005t0023g0094a0004c0005t0023g0095a0004c0005t0039g0084others(3): Show | 6 | HG00642.hp2 HG01081.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.3737-1711dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16805873 | |||||
| chr19:16805876
|
C | T | 53 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(50): Show | 53 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.3737-1710C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805876 | ||||||
| chr19:16805901
|
A | G | 9 | a0001c0002t0004g0011a0002c0001t0003g0176a0002c0001t0003g0183others(6): Show | 9 | HG01081.hp2 HG01257.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.3737-1685A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16805901 | ||||||
| chr19:16806084
|
A | G | 67 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(64): Show | 67 | HG00609.hp2 HG00642.hp2 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.3737-1502A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806084 | ||||||
| chr19:16806311
|
C | T | 3 | a0013c0018t0017g0294a0013c0018t0017g0295a0013c0018t0022g0124 | 3 | HG03098.hp1 HG03471.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3737-1275C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806311 | ||||||
| chr19:16806646
|
G | A | 3 | a0006c0015t0028g0204a0039c0057t0026g0202a0041c0065t0032g0166 | 3 | HG01884.hp1 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3737-940G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806646 | ||||||
| chr19:16806740
|
C | T | 2 | a0003c0006t0038g0106a0044c0058t0035g0167 | 2 | HG02148.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3737-846C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806740 | ||||||
| chr19:16806879
|
T | C | 1 | a0004c0005t0006g0229 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3737-707T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16806879 | ||||||
| chr19:16807137
|
T | C | 1 | a0002c0001t0002g0043 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3737-449T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807137 | ||||||
| chr19:16807145
|
G | A | 1 | a0004c0060t0002g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3737-441G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807145 | ||||||
| chr19:16807170
|
CA | C | 48 | a0001c0008t0001g0270a0002c0007t0002g0008a0003c0003t0046g0077others(45): Show | 48 | HG00597.hp1 HG00642.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.3737-399delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16807170 | |||||
| chr19:16807170
|
CAA | C | 16 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(13): Show | 16 | HG00609.hp2 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.3737-400_3737-399d others(4): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr19 | 16807170 | |||||
| chr19:16807285
|
G | A | 12 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0002t0001g0191others(9): Show | 12 | HG00544.hp2 HG00673.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.3737-301G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807285 | ||||||
| chr19:16807325
|
C | A | 5 | a0001c0002t0001g0199a0001c0002t0001g0268a0001c0002t0012g0188others(2): Show | 5 | HG02071.hp1 HG02080.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.3737-261C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807325 | ||||||
| chr19:16807512
|
A | G | 1 | a0003c0059t0015g0037 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3737-74A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807512 | ||||||
| chr19:16807516
|
A | C | 7 | a0004c0009t0009g0047a0010c0013t0013g0172a0010c0013t0013g0173others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.3737-70A>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 17/18 | chr19 | 16807516 | ||||||
| chr19:16808230
|
G | A | 1 | a0001c0002t0002g0013 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4287+94G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808230 | ||||||
| chr19:16808232
|
C | T | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4287+96C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808232 | ||||||
| chr19:16808237
|
A | G | 1 | a0001c0002t0002g0123 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.4287+101A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808237 | ||||||
| chr19:16808378
|
C | T | 1 | a0003c0003t0002g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4287+242C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808378 | ||||||
| chr19:16808549
|
A | AAAAAG | 7 | a0004c0005t0029g0265a0006c0015t0028g0204a0015c0020t0007g0119others(4): Show | 7 | HG01884.hp1 HG02040.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.4287+434_4287+438d others(7): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16808549 | |||||
| chr19:16808614
|
A | T | 2 | a0004c0005t0023g0094a0004c0005t0023g0095 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4287+478A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808614 | ||||||
| chr19:16808645
|
G | A | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4287+509G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808645 | ||||||
| chr19:16808720
|
G | A | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4287+584G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808720 | ||||||
| chr19:16808827
|
C | T | 20 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(17): Show | 20 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.4287+691C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16808827 | ||||||
| chr19:16809095
|
A | AT | 17 | a0001c0002t0003g0186a0001c0002t0004g0011a0002c0001t0003g0176others(14): Show | 17 | HG01081.hp2 HG01257.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.4287+971dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809095 | |||||
| chr19:16809195
|
C | T | 42 | a0001c0002t0020g0249a0002c0001t0020g0289a0003c0003t0044g0070others(39): Show | 42 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4287+1059C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809195 | ||||||
| chr19:16809200
|
C | T | 1 | a0044c0058t0035g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4287+1064C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809200 | ||||||
| chr19:16809541
|
T | C | 2 | a0002c0001t0003g0177a0002c0001t0003g0182 | 2 | NA18952.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.4287+1405T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809541 | ||||||
| chr19:16809553
|
CTTTTTCT others(5): Show |
C | 17 | a0004c0005t0006g0211a0004c0005t0006g0225a0004c0005t0006g0226others(14): Show | 17 | HG01884.hp2 HG02055.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4287+1423_4287+143 others(16): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809553 | |||||
| chr19:16809559
|
C | CT | 9 | a0004c0005t0029g0265a0006c0015t0028g0204a0011c0011t0002g0022others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4287+1436dupT | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809559 | |||||
| chr19:16809559
|
CTTTTTT | C | 33 | a0001c0002t0020g0249a0002c0001t0020g0289a0003c0003t0044g0070others(30): Show | 33 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.4287+1431_4287+143 others(10): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16809559 | |||||
| chr19:16809585
|
T | C | 42 | a0001c0002t0020g0249a0002c0001t0020g0289a0003c0003t0044g0070others(39): Show | 42 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.4287+1449T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809585 | ||||||
| chr19:16809647
|
C | T | 5 | a0004c0005t0029g0265a0006c0015t0028g0204a0038c0049t0042g0054others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4287+1511C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809647 | ||||||
| chr19:16809703
|
C | T | 2 | a0039c0057t0026g0202a0041c0065t0032g0166 | 2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4287+1567C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809703 | ||||||
| chr19:16809711
|
C | T | 3 | a0004c0005t0001g0296a0009c0068t0040g0116a0014c0054t0025g0118 | 3 | HG02896.hp1 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4287+1575C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809711 | ||||||
| chr19:16809835
|
T | G | 1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4287+1699T>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809835 | ||||||
| chr19:16809836
|
C | T | 1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4287+1700C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809836 | ||||||
| chr19:16809837
|
A | G | 1 | a0002c0001t0001g0147 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4287+1701A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809837 | ||||||
| chr19:16809838
|
T | C | 4 | a0011c0011t0002g0022a0011c0011t0011g0017a0011c0011t0011g0024others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+1702T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809838 | ||||||
| chr19:16809861
|
C | T | 4 | a0011c0011t0002g0022a0011c0011t0011g0017a0011c0011t0011g0024others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4287+1725C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809861 | ||||||
| chr19:16809903
|
T | A | 3 | a0001c0002t0020g0249a0002c0001t0020g0289a0003c0003t0044g0070 | 3 | HG01099.hp2 HG01192.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4287+1767T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16809903 | ||||||
| chr19:16810049
|
G | T | 125 | a0001c0002t0001g0142a0001c0002t0001g0153a0001c0002t0001g0154others(122): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.4287+1913G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810049 | ||||||
| chr19:16810332
|
G | C | 5 | a0004c0005t0029g0265a0006c0015t0028g0204a0038c0049t0042g0054others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4287+2196G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810332 | ||||||
| chr19:16810386
|
C | T | 6 | a0001c0002t0001g0146a0001c0002t0001g0157a0001c0002t0001g0165others(3): Show | 6 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.4287+2250C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810386 | ||||||
| chr19:16810395
|
G | A | 21 | a0004c0009t0008g0205a0004c0009t0008g0286a0004c0009t0009g0047others(18): Show | 21 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.4287+2259G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810395 | ||||||
| chr19:16810437
|
C | CA | 50 | a0001c0002t0001g0146a0001c0002t0001g0157a0001c0002t0001g0165others(47): Show | 50 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.4287+2321dupA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16810437 | |||||
| chr19:16810437
|
C | CAA | 45 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(42): Show | 45 | HG00609.hp2 HG00735.hp2 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.4287+2320_4287+232 others(6): Show |
NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16810437 | |||||
| chr19:16810454
|
A | G | 12 | a0004c0005t0006g0211a0004c0005t0006g0225a0004c0005t0006g0226others(9): Show | 12 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.4287+2318A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810454 | ||||||
| chr19:16810651
|
T | C | 1 | a0001c0002t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4287+2515T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810651 | ||||||
| chr19:16810652
|
A | T | 1 | a0001c0002t0001g0181 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4287+2516A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810652 | ||||||
| chr19:16810719
|
C | T | 9 | a0004c0005t0029g0265a0006c0015t0028g0204a0011c0011t0002g0022others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4287+2583C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810719 | ||||||
| chr19:16810745
|
G | T | 3 | a0002c0001t0005g0155a0002c0001t0005g0245a0002c0001t0014g0187 | 3 | HG00558.hp1 HG02027.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.4287+2609G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810745 | ||||||
| chr19:16810774
|
T | C | 1 | a0003c0006t0002g0096 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4287+2638T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810774 | ||||||
| chr19:16810951
|
C | T | 41 | a0001c0002t0001g0153a0001c0002t0001g0154a0001c0002t0001g0181others(38): Show | 41 | HG00280.hp2 HG00558.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.4287+2815C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16810951 | ||||||
| chr19:16811252
|
A | T | 3 | a0001c0002t0020g0249a0002c0001t0020g0289a0003c0003t0044g0070 | 3 | HG01099.hp2 HG01192.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4287+3116A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811252 | ||||||
| chr19:16811323
|
C | T | 30 | a0004c0005t0001g0296a0004c0005t0018g0256a0004c0005t0023g0094others(27): Show | 30 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.4287+3187C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811323 | ||||||
| chr19:16811441
|
G | A | 17 | a0001c0002t0002g0013a0001c0022t0001g0151a0001c0022t0002g0102others(14): Show | 17 | HG00609.hp2 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.4287+3305G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811441 | ||||||
| chr19:16811447
|
G | C | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4287+3311G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811447 | ||||||
| chr19:16811485
|
G | T | 2 | a0001c0002t0007g0030a0015c0020t0045g0121 | 2 | NA18951.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.4287+3349G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16811485 | ||||||
| chr19:16811586
|
GA | G | 10 | a0002c0001t0004g0112a0002c0001t0005g0155a0002c0001t0014g0187others(7): Show | 10 | HG01070.hp2 HG01257.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.4288-3428delA | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr19 | 16811586 | |||||
| chr19:16812104
|
T | A | 1 | a0003c0003t0002g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4288-2924T>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812104 | ||||||
| chr19:16812360
|
A | T | 4 | a0011c0011t0002g0022a0011c0011t0011g0017a0011c0011t0011g0024others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4288-2668A>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812360 | ||||||
| chr19:16812378
|
T | C | 1 | a0002c0001t0001g0261 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4288-2650T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812378 | ||||||
| chr19:16812402
|
C | T | 1 | a0012c0017t0001g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4288-2626C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812402 | ||||||
| chr19:16812538
|
T | C | 6 | a0001c0002t0001g0291a0001c0002t0002g0007a0002c0001t0001g0242others(3): Show | 6 | NA18954.hp2 NA18968.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.4288-2490T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812538 | ||||||
| chr19:16812683
|
C | G | 146 | a0001c0002t0001g0146a0001c0002t0001g0148a0001c0002t0001g0157others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.4288-2345C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812683 | ||||||
| chr19:16812954
|
C | G | 1 | a0003c0006t0002g0086 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.4288-2074C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812954 | ||||||
| chr19:16812967
|
C | T | 1 | a0001c0002t0001g0179 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4288-2061C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16812967 | ||||||
| chr19:16813038
|
C | T | 1 | a0001c0002t0001g0199 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4288-1990C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813038 | ||||||
| chr19:16813055
|
G | A | 1 | a0008c0010t0047g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4288-1973G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813055 | ||||||
| chr19:16813177
|
G | C | 1 | a0005c0004t0003g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4288-1851G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813177 | ||||||
| chr19:16813444
|
G | C | 1 | a0002c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4288-1584G>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813444 | ||||||
| chr19:16813445
|
C | G | 1 | a0002c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4288-1583C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813445 | ||||||
| chr19:16813447
|
T | C | 1 | a0002c0001t0033g0216 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4288-1581T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813447 | ||||||
| chr19:16813618
|
G | A | 1 | a0001c0033t0002g0012 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4288-1410G>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813618 | ||||||
| chr19:16813714
|
T | C | 5 | a0004c0005t0029g0265a0006c0015t0028g0204a0038c0049t0042g0054others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.4288-1314T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813714 | ||||||
| chr19:16813740
|
G | T | 1 | a0002c0001t0001g0164 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.4288-1288G>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16813740 | ||||||
| chr19:16814030
|
T | C | 9 | a0004c0005t0029g0265a0006c0015t0028g0204a0011c0011t0002g0022others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4288-998T>C | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814030 | ||||||
| chr19:16814118
|
C | A | 9 | a0004c0005t0029g0265a0006c0015t0028g0204a0011c0011t0002g0022others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4288-910C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814118 | ||||||
| chr19:16814141
|
C | A | 4 | a0012c0017t0001g0212a0012c0017t0002g0018a0012c0017t0002g0019others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.4288-887C>A | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814141 | ||||||
| chr19:16814381
|
C | T | 2 | a0009c0068t0040g0116a0014c0054t0025g0118 | 2 | HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4288-647C>T | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814381 | ||||||
| chr19:16814584
|
A | G | 1 | a0041c0065t0032g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4288-444A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814584 | ||||||
| chr19:16814781
|
C | G | 1 | a0003c0003t0002g0076 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4288-247C>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814781 | ||||||
| chr19:16814862
|
A | G | 9 | a0004c0005t0029g0265a0006c0015t0028g0204a0011c0011t0002g0022others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.4288-166A>G | NWD1 | ENSG00000188039.17 | transcript | ENST00000524140.7 | protein_coding | 18/18 | chr19 | 16814862 |